(3S)-3-氨基-1-苄基吡咯烷-2,5-二酮

反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: Into a 200 ml four-necked flask with a stirrer, a dropping funnel, a Dimroth condenser, and a thermometer, 9.5 g (46.5mmol) of the (S)-1-benzyl-3-aminopyrrolidine-2,5-dione, 50 ml of tetrahydrofuran, and 8.8 g (0.23 mol) of sodium borohydride were introduced, and a solution in which 11.5g (0.12 mol) of 98% sulfuric acid were diluted with 20 ml of tetrahydrofuran was added dropwise over approximately 30 minutes while stirring under an ice-bath, and then stirring was performed for 2 hours. The reaction mixture was heated to 65° C. and was stirred for 2 hours. After the reaction was complete, vacuum concentration was performed. 70 g of water was added for dissolution, and 25 g of concentrated hydrochloric acid were added thereto, followed by stirring at 65° C. for 4 hours. The reaction mixture was cooled to room temperature and was neutralized by adding 32 g of 46% sodium hydroxide while stirring. Extraction was performed three times using 100 ml of toluene, and all the toluene layers were simultaneously subjected to vacuum concentration. The concentrate was subjected to vacuum distillation, and thus 7.3 g of (S)-1-benzyl-3-aminopyrrolidine were obtained as the distillate collected at 130 to 133° C./1.3 kPa. As a result of analysis, the chemical purity was 99% and the optical purity was 91% e.e. 7.0 g of the (S)-1-benzyl-3-aminopyrrolidine, 25 ml of methanol, and 0.7 g of 5% Pd/C were introduced into a 100 ml autoclave, and hydrogen was adjusted to have a pressure of 1 MPa. The temperature was increased to 70° C. and stirring was performed for 8 hours. After the reaction was complete, the temperature was decreased to room temperature and the pressure was released. The content was filtered and the mother liquor was concentrated and distilled, and thus 3.2 g of (S)-3-aminopyrrolidine were obtained as the distillate collected at 80 to 83° C./40 kPa. As a result of analysis, the chemical purity was 99% and the optical purity was 90% e.e. was added dropwise over approximately 30 minutes stirring was stirred for 2 hours vacuum concentration 70 g of water was added for dissolution, and 25 g of concentrated hydrochloric acid were added by stirring at 65° C. for 4 hours The reaction mixture was cooled to room temperature by adding 32 g of 46% sodium hydroxide while stirring Extraction all the toluene layers were simultaneously subjected to vacuum concentration The concentrate was subjected to vacuum distillation