methyl 3-chloro-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

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

Procedure: A solution of triphenylphosphine (65.8 g, 0.251 mol)) and hexachloroethane (59.4 g, 0.251 mol) in dichloromethane (850 mL) was added in one portion to a solution of N-Boc-serine methyl ester (50 g, 0.228 mol) in dichloromethane (170 mL) under argon atmosphere. The reaction mixture was stirred at room temperature for 2 h and then the reaction was quenched with a saturated solution of NaHCO3 (150 mL). The organic product was extracted with dichloromethane (2×300 mL) and the combined organic layers was washed with brine (300 mL) and dried over anhydrous sodium sulphate. The solution was concentrated under reduced pressure and then triturated with Et2O (500 mL). After filtration and evaporation of the solvent, the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet ether) which gave the title compound (42 g, 78%). the reaction was quenched with a saturated solution of NaHCO3 (150 mL) The organic product was extracted with dichloromethane (2×300 mL) the combined organic layers was washed with brine (300 mL) dried over anhydrous sodium sulphate The solution was concentrated under reduced pressure triturated with Et2O (500 mL) After filtration and evaporation of the solvent the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet ether) which

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

Procedure: A solution of triphenylphosphine (65.8 g, 0.251 mol)) and hexachloroethane (59.4 g, 0.251 mol) in dichloromethane (850 mL) was added in one portion to a solution of N-Boc-serine methyl ester (50 g, 0.228 mol) in dichloromethane (170 mL) under argon atmosphere. The reaction mixture was stirred at room temperature for 2 h and then the reaction was quenched with a saturated solution of NaHCO3 (150 mL). The organic product was extracted with dichloromethane (2×300 mL) and the combined organic layers was washed with brine (300 mL) and dried over anhydrous sodium sulphate. The solution was concentrated under reduced pressure and then triturated with Et2O (500 mL). After filtration and evaporation of the solvent, the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet. ether) which gave the title compound (42 g, 78%). the reaction was quenched with a saturated solution of NaHCO3 (150 mL) The organic product was extracted with dichloromethane (2×300 mL) the combined organic layers was washed with brine (300 mL) dried over anhydrous sodium sulphate The solution was concentrated under reduced pressure triturated with Et2O (500 mL) After filtration and evaporation of the solvent the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet. ether) which

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

Procedure: A solution of triphenylphosphine (65.8 g, 0.251 mol)) and hexachloroethane (59.4 g, 0.251 mol) in dichloromethane (850 mL) was added in one portion to a solution of N-Boc-serine methyl ester (50 g, 0.228 mol) in dichloromethane (170 mL) under argon atmosphere. The reaction mixture was stirred at room temperature for 2 h and then the reaction was quenched with a saturated solution of NaHCO3 (150 mL). The organic product was extracted with dichloromethane (2×300 mL) and the combined organic layers was washed with brine (300 mL) and dried over anhydrous sodium sulphate. The solution was concentrated under reduced pressure and then triturated with Et2O (500 mL). After filtration and evaporation of the solvent, the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet. ether) which gave the title compound (42 g, 78%). the reaction was quenched with a saturated solution of NaHCO3 (150 mL) The organic product was extracted with dichloromethane (2×300 mL) the combined organic layers was washed with brine (300 mL) dried over anhydrous sodium sulphate The solution was concentrated under reduced pressure triturated with Et2O (500 mL) After filtration and evaporation of the solvent the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet. ether) which

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

Procedure: A solution of triphenylphosphine (65.8 g, 0.251 mol)) and hexachloroethane (59.4 g, 0.251 mol) in dichloromethane (850 mL) was added in one portion to a solution of N-Boc-serine methyl ester (50 g, 0.228 mol) in dichloromethane (170 mL) under argon atmosphere. The reaction mixture was stirred at room temperature for 2 h and then the reaction was quenched with a saturated solution of NaHCO3 (150 mL). The organic product was extracted with dichloromethane (2×300 mL) and the combined organic layers was washed with brine (300 mL) and dried over anhydrous sodium sulphate. The solution was concentrated under reduced pressure and then triturated with Et2O (500 mL). After filtration and evaporation of the solvent, the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet ether) which gave the title compound (42 g, 78%). the reaction was quenched with a saturated solution of NaHCO3 (150 mL) The organic product was extracted with dichloromethane (2×300 mL) the combined organic layers was washed with brine (300 mL) dried over anhydrous sodium sulphate The solution was concentrated under reduced pressure triturated with Et2O (500 mL) After filtration and evaporation of the solvent the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet ether) which

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

Procedure: A solution of triphenylphosphine (65.8 g, 0.251 mol)) and hexachloroethane (59.4 g, 0.251 mol) in dichloromethane (850 mL) was added in one portion to a solution of N-Boc-serine methyl ester (50 g, 0.228 mol) in dichloromethane (170 mL) under argon atmosphere. The reaction mixture was stirred at room temperature for 2 h and then the reaction was quenched with a saturated solution of NaHCO3 (150 mL). The organic product was extracted with dichloromethane (2×300 mL) and the combined organic layers was washed with brine (300 mL) and dried over anhydrous sodium sulphate. The solution was concentrated under reduced pressure and then triturated with Et2O (500 mL). After filtration and evaporation of the solvent, the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet ether) which gave the title compound (42 g, 78%). the reaction was quenched with a saturated solution of NaHCO3 (150 mL) The organic product was extracted with dichloromethane (2×300 mL) the combined organic layers was washed with brine (300 mL) dried over anhydrous sodium sulphate The solution was concentrated under reduced pressure triturated with Et2O (500 mL) After filtration and evaporation of the solvent the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet ether) which

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

Procedure: A solution of triphenylphosphine (65.8 g, 0.251 mol)) and hexachloroethane (59.4 g, 0.251 mol) in dichloromethane (850 mL) was added in one portion to a solution of N-Boc-serine methyl ester (50 g, 0.228 mol) in dichloromethane (170 mL) under argon atmosphere. The reaction mixture was stirred at room temperature for 2 h and then the reaction was quenched with a saturated solution of NaHCO3 (150 mL). The organic product was extracted with dichloromethane (2×300 mL) and the combined organic layers was washed with brine (300 mL) and dried over anhydrous sodium sulphate. The solution was concentrated under reduced pressure and then triturated with Et2O (500 mL). After filtration and evaporation of the solvent, the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet. ether) which gave the title compound (42 g, 78%). the reaction was quenched with a saturated solution of NaHCO3 (150 mL) The organic product was extracted with dichloromethane (2×300 mL) the combined organic layers was washed with brine (300 mL) dried over anhydrous sodium sulphate The solution was concentrated under reduced pressure triturated with Et2O (500 mL) After filtration and evaporation of the solvent the crude product was purified by chromatography on a silica column eluted with 6-8% EtOAc in pet. ether) which