ethyl 2-diethoxyphosphoryl-3-methylbutanoate

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 123 mg of lithium chloride was suspended in 10 ml of dry tetrahydrofuran under an argon stream, and 0.69 ml of ethyl 2-diethylphosphono-3-methylbutanoate was added under stirring. The mixture was stirred for 5 minutes at room temperature, and then 2.7 ml of a 20% dry tetrahydrofuran solution of diazabicycloundecene was added thereto. The mixture was stirred at room temperature for 10 minutes. Then, 2.0 ml of a dry tetrahydrofuran solution of 773 mg of (4S,5R)-3-benzyloxycarbonyl-2,2-dimethyl-5-formyl-4-isobutyloxazolidine was added thereto, and the mixture was stirred overnight at room temperature. A precipitated inorganic salt was filtered off, and the solvent of the filtrate was distilled off under reduced pressure. The residue was dissolved in 300 ml of benzene and washed with 200 ml of water. The separated aqueous layer was extracted with 75 ml of benzene. The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) by using a mixture of hexane/ethyl acetate (10/1) to obtain 623 mg of ethyl 3-[(4S,5S)-3-benzyloxycarbonyl-2,2-dimethyl-4-isobutyloxazolidin-5-yl]-2-isopropyl-2-propenoate as a colorless oily substance. was added The mixture was stirred for 5 minutes at room temperature The mixture was stirred at room temperature for 10 minutes the mixture was stirred overnight at room temperature A precipitated inorganic salt was filtered off the solvent of the filtrate was distilled off under reduced pressure The residue was dissolved in 300 ml of benzene washed with 200 ml of water The separated aqueous layer was extracted with 75 ml of benzene The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate Then, the solvent was distilled off under reduced pressure the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) a mixture of hexane/ethyl acetate (10/1)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 123 mg of lithium chloride was suspended in 10 ml of dry tetrahydrofuran under an argon stream, and 0.69 ml of ethyl 2-diethylphosphono-3-methylbutanoate was added under stirring. The mixture was stirred for 5 minutes at room temperature, and then 2.7 ml of a 20% dry tetrahydrofuran solution of diazabicycloundecene was added thereto. The mixture was stirred at room temperature for 10 minutes. Then, 2.0 ml of a dry tetrahydrofuran solution of 773 mg of (4S,5R)-3-benzyloxycarbonyl-2,2-dimethyl-5-formyl-4-isobutyloxazolidine was added thereto, and the mixture was stirred overnight at room temperature. A precipitated inorganic salt was filtered off, and the solvent of the filtrate was distilled off under reduced pressure. The residue was dissolved in 300 ml of benzene and washed with 200 ml of water. The separated aqueous layer was extracted with 75 ml of benzene. The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) by using a mixture of hexane/ethyl acetate (10/1) to obtain 623 mg of ethyl 3-[(4S,5S)-3-benzyloxycarbonyl-2,2-dimethyl-4-isobutyloxazolidin-5-yl]-2-isopropyl-2-propenoate as a colorless oily substance. was added The mixture was stirred for 5 minutes at room temperature The mixture was stirred at room temperature for 10 minutes the mixture was stirred overnight at room temperature A precipitated inorganic salt was filtered off the solvent of the filtrate was distilled off under reduced pressure The residue was dissolved in 300 ml of benzene washed with 200 ml of water The separated aqueous layer was extracted with 75 ml of benzene The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate Then, the solvent was distilled off under reduced pressure the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) a mixture of hexane/ethyl acetate (10/1)

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Using the procedure described in Example 31 (Step 3), reaction of 4-(6-Methoxy-3-methyl-2-phenyl-naphthalen-1-yloxy)-benzaldehyde (8) (0.507 g, 1.38 mmol), 2-(diethoxy-phosphoryl)-3-methyl-butyric acid ethyl ester (1.1 g, 4.13 mmol) and 1.6 M nBuLi (2.8 mL, 4.41 mmol) in dry THF (14 mL) afforded 2 isomeric products (222) as oils. Yield: (222-1) Isomer (1) 0.177 (27%); (222-2) Isomer (2) 0.195 g (30%). Isomer (1): 1H NMR (400 MHz, d-CDCl3): δ 1.20 (d, J=6.9 Hz, 6H), 1.32 (t, J=7.1 Hz, 3H), 2.24 (s, 3H), 3.06-3.10 (m, 1H), 3.94 (s, 3H), 4.20-4.25 (m, 2H), 6.58 (d, J=8.8 Hz, 2H), 7.03-7.07 (m, 3H), 7.12-7.14 (m, 3H), 7.22-7.26 (m, 3H), 7.39 (s, 1H), 7.56 (s, 1H), 7.78 (d, J=9.1 Hz, 1H).

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 123 mg of lithium chloride was suspended in 10 ml of dry tetrahydrofuran under an argon atmosphere, and 0.69 ml of ethyl 2-diethylphosphono-3-methylbutanoate was added thereto under stirring. Then, 2.7 ml of a 20% dry tetrahydrofuran solution of diazabicycloundecene was added thereto and stirred for 10 minutes at room temperature. A solution prepared by dissolving 773 mg of (4S,5R)-3-benzyloxycarbonyl-2,2-dimethyl-5-formyl-4-isobutyloxazolidine in dry tetrahydrofuran was gradually dropwise added thereto, and the mixture was stirred overnight at room temperature. The inorganic salt precipitated was filtered off and the solvent was distilled off under reduced pressure. The residue was dissolved in 300 ml of benzene, washed with water and dried oer anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (32 g of Kiesel gel 60) by using a mixture of n-hexane/ethyl acetate (10/1) to obtain 623 mg of ethyl 3-[(4S,5S)-3-benzyloxycarbonyl-2,2-dimethyl-4-isobutyloxazolidin-5-yl]-2-isopropyl-2-propenoate as a colorless oily substance. stirred for 10 minutes at room temperature A solution prepared was gradually dropwise added the mixture was stirred overnight at room temperature The inorganic salt precipitated was filtered off the solvent was distilled off under reduced pressure The residue was dissolved in 300 ml of benzene washed with water dried oer anhydrous magnesium sulfate The solvent was distilled off under reduced pressure the residue was purified by silica gel column chromatography (32 g of Kiesel gel 60) a mixture of n-hexane/ethyl acetate (10/1)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 123 mg of lithium chloride was suspended in 10 ml of dry tetrahydrofuran under an argon stream, and 0.69 ml of ethyl 2-diethylphosphono-3-methylbutanoate was added under stirring. The mixture was stirred for 5 minutes at room temperature, and then 2.7 ml of a 20% dry tetrahydrofuran solution of diazabicycloundecene was added thereto. The mixture was stirred at room temperature for 10 minutes. Then, 2.0 ml of a dry tetrahydrofuran solution of 773 mg of (4S,5R)-3-benzyloxycarbonyl-2,2-dimethyl-5-formyl-4-isobutyloxazolidine was added thereto, and the mixture was stirred overnight at room temperature. A precipitated inorganic salt was filtered off, and the solvent of the filtrate was distilled off under reduced pressure. The residue was dissolved in 300 ml of benzene and washed with 200 ml of water. The separated aqueous layer was extracted with 75 ml of benzene. The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) by using a mixture of hexane/ethyl acetate (10/1) to obtain 623 mg of ethyl 3-[(4S,5S)-3-benzyloxycarbonyl-2,2-dimethyl-4-isobutyloxazolidin-5-yl]-2-isopropyl-2-propenoate as a colorless oily substance. was added The mixture was stirred for 5 minutes at room temperature The mixture was stirred at room temperature for 10 minutes the mixture was stirred overnight at room temperature A precipitated inorganic salt was filtered off the solvent of the filtrate was distilled off under reduced pressure The residue was dissolved in 300 ml of benzene washed with 200 ml of water The separated aqueous layer was extracted with 75 ml of benzene The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate Then, the solvent was distilled off under reduced pressure the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) a mixture of hexane/ethyl acetate (10/1)