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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 843694생성일: 2026년 10월 26일

Benzylamine → Benzyl isovalerate

https://huagongshe.com/reaction/843694

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
용매DichloromethaneHCID 6344—
생성물Benzyl isovalerateHCID 7651—

반응 단계

To a solution of 2-(R)-2-[carboxymethyl(4-methoxybenzenesulfonyl)amino]-3-methylbutyric acid benzyl ester (example 1) (905 mg, 2.08 mmol) in methylene chloride (18 mL) were added sequentially triethylamine (0.72 mL, 5.14 mmol), benzylamine (0.25 mL, 2.29 mmol) and (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (1.01 grams, 2.28 mmol). The mixture was stirred at room temperature overnight and then diluted with ethyl acetate. The solution was washed with 0.5 N hydrochloric acid solution and brine, dried over magnesium sulfate and concentrated under vacuum. The residue was chromatographed on silica gel using a 2:5:16 ratio of methylene chloride/ethyl acetate/hexane affording 2-(R)-2-[benzylcarbamoylmethyl)(4-methoxybenzenesulfonyl)amino]-3-methylbutyric acid benzyl ester as a clear oil, 933 mg (86%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380219B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-52a75c38a59a40fb8215132dd525dc6a
출처 메모uspto-grants-2002_04