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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271611생성일: 2026년 10월 27일

4-Chlorobenzaldehyde → (R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl ester

https://huagongshe.com/reaction/271611

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzaldehydeHCID 7726—
반응물TriethylamineHCID 8471—
반응물Sodium borohydrideHCID 4311764—
반응물Methyl D-valinate hydrochlorideHCID 11984198—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매Sulfuric acid magnesium salt (1:1)HCID 24083—
생성물(R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl esterHCID 815060197%

반응 단계

3 g (18 mmoles) of (R)-2-amino-3-methyl-butyric acid methyl ester hydrochloride, 2.1 g (15 mmoles) of 4-chloro-benzaldehyde and 2.94 ml (21 mmoles) of triethyl amine are dissolved in 100 ml of CH2Cl2 and excess of MgSO4 is added at ambient temperature under N2 atmosphere. After being stirred for 18 hours at ambient temperature, the reaction mixture is filtered off and washed with CH2Cl2. The filtrate is concentrated under reduced pressure. To the crude imine in 250 ml of MeOH, 2.04 g (54 mmoles) of NaBH4 is added portionwise at 0° C. The reaction mixture is stirred at 0° C. for 2 hours and concentrated to ¼ of whole volume under reduced pressure. The mixture is extracted with AcOEt and the combined extracts are washed with sat. NaHCO3 and brine, dried over Na2SO4 and concentrated under reduced pressure to give 3.72 g of desired (R)-2-(4-chloro-benzylamino)-3-methyl-butyric acid methyl ester in 97% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452886B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-aca9aa7d68bd4897b31cc18c0fd04ce7
출처 메모uspto-grants-2008_11