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HRID 2044128생성일: 2026년 10월 27일

Acetyl chloride → Methyl 4-bromo-2-amino-butyrate hydrochloride

https://huagongshe.com/reaction/2044128

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물2-Amino-4-bromobutanoic acid hydrobromideHCID 13877992—
용매MethanolHCID 887—
생성물Methyl 4-bromo-2-amino-butyrate hydrochlorideHCID 1387799382%

반응 단계

A suspension of α-amino-γ-butyrolactone hydrobromide in 30% HBr in HOAc is heated at 100° C. in a sealed tube for 5 days. The mixture is concentrated to give a white solid that is washed with ether to provide 23.1 g (64%) of 2-amino-4-bromo-butyric acid hydrobromide. Acetyl chloride (61 mL, 860 mmol) is added dropwise to 200 mL of MeOH at 0° C. The mixture is stirred at rt for 30 min before 22.5 g (124 mmol) of 2-amino-4-bromo-butyric acid hydrobromide is added. The mixture is stirred overnight and concentrated. The residue is washed with ether to provide 23.5 g (82%) of methyl 4-bromo-2-amino-butyrate hydrochloride. A solution of 27.7 g (330 mmol) of NaHCO3 in 100 mL of water is slowly added to 19.2 g (82.5 mmol) of this material along with 21.6 g (99.0 mmol) of Boc2O in 140 mL of 1,4-dioxane at 0° C. The mixture is warmed to rt and stirred overnight. N,N-dimethyl propane-1,3-diamine (5 mL) is added to the mixture, and it is stirred for 20 min. The mixture is diluted with water then extracted twice with EtOAc. The extracts are washed with water, 1M NaHSO4, and brine, and then combined, dried with Na2SO4, filtered, and concentrated to provide 21.5 g (88%) of I-042 as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08586748B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-46cdffebf1834014a3fe086a2df6b102
출처 메모uspto-grants-2013_11