4-(diethylamino)but-2-yn-1-ol

Conditions: temp:92.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 204 parts by weight of aqueous 55% strength propargyl alcohol, 250 parts by weight of 30% strength aqueous formaldehyde, 161 parts by weight of diethylamine, 1.4 parts by weight of copper sulfate, 2 parts by weight of potassium iodide, 50 parts by weight of water and 115 parts by weight of concentrated sulfuric acid are mixed and brought to pH 5. The mixture is heated for 5 hours at 92° C. and worked up as described. 242 parts by weight of 1-diethylaminobut-2-yn-4-ol are obtained, corresponding to a yield of 86%.

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

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

Procedure: To a solution of 4-diethylamino-2-butyn-1-ol (1.00 g, 7.08 mmol) in anhydrous DCM (60 mL) was added MnO2 (20 g, 230 mmol) portion wise on one hour. The resulting mixture was stirred at rt for two additional hours, then filtered on a bed of Celite. The filtrates were evaporated under reduced pressure to give 352 mg (36%) the title compound as an orange oil (352 mg, 36% yield). 1H NMR (CDCl3) δ: 9.22 (s, 1H), 3.65 (s, 2H), 2.58 (q, J=7.2 Hz, 4H), 1.08 (t, J=7.2 Hz, 6H). filtered on a bed of Celite The filtrates were evaporated under reduced pressure

Conditions: temp:92.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 204 parts by weight of aqueous 55% strength propargyl alcohol, 250 parts by weight of 30% strength aqueous formaldehyde, 161 parts by weight of diethylamine, 1.4 parts by weight of copper sulfate, 2 parts by weight of potassium iodide, 50 parts by weight of water and 115 parts by weight of concentrated sulfuric acid are mixed and brought to pH 5. The mixture is heated for 5 hours at 92° C. and worked up as described. 242 parts by weight of 1-diethylaminobut-2-yn-4-ol are obtained, corresponding to a yield of 86%.

Conditions: temp:92.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 204 parts by weight of aqueous 55% strength propargyl alcohol, 250 parts by weight of 30% strength aqueous formaldehyde, 161 parts by weight of diethylamine, 1.4 parts by weight of copper sulfate, 2 parts by weight of potassium iodide, 50 parts by weight of water and 115 parts by weight of concentrated sulfuric acid are mixed and brought to pH 5. The mixture is heated for 5 hours at 92° C. and worked up as described. 242 parts by weight of 1-diethylaminobut-2-yn-4-ol are obtained, corresponding to a yield of 86%.

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

Conditions: temp:92.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: 204 parts by weight of aqueous 55% strength propargyl alcohol, 250 parts by weight of 30% strength aqueous formaldehyde, 161 parts by weight of diethylamine, 1.4 parts by weight of copper sulfate, 2 parts by weight of potassium iodide, 50 parts by weight of water and 115 parts by weight of concentrated sulfuric acid are mixed and brought to pH 5. The mixture is heated for 5 hours at 92° C. and worked up as described. 242 parts by weight of 1-diethylaminobut-2-yn-4-ol are obtained, corresponding to a yield of 86%.

Conditions: temp:62.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of para formaldehyde (105.0 g), N,N-diethyl amine (300 g) and copper(II) acetate (7.5 g) in 1,4 dioxane (900 ml) was heated to 60-65° C. After 1.5 h, 2-propyne-1-ol (150 g, 2.7 moles) was added and the mixture was heated at 90-95° C. after 2 hrs; excess solvent, 1,4 dioxane, evaporated at reduced pressure to afford 315 g (84%) of the product as an oil. the mixture was heated at 90-95° C. after 2 hrs excess solvent, 1,4 dioxane, evaporated at reduced pressure

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

Procedure: To a solution of 4-diethylamino-2-butyn-1-ol (1.00 g, 7.08 mmol) in anhydrous DCM (60 mL) was added MnO2 (20 g, 230 mmol) portion wise on one hour. The resulting mixture was stirred at rt for two additional hours, then filtered on a bed of Celite. The filtrates were evaporated under reduced pressure to give 352 mg (36%) the title compound as an orange oil (352 mg, 36% yield). 1H NMR (CDCl3) δ: 9.22 (s, 1H), 3.65 (s, 2H), 2.58 (q, J=7.2 Hz, 4H), 1.08 (t, J=7.2 Hz, 6H). filtered on a bed of Celite The filtrates were evaporated under reduced pressure