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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 278461생성일: 2026년 10월 25일

Triethylamine → Ethyl (alphaR)-alpha-[(methylsulfonyl)oxy]benzenebutanoate

https://huagongshe.com/reaction/278461

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Ethyl (R)-2-hydroxy-4-phenylbutyrateHCID 2733848—
용매DichloromethaneHCID 6344—
생성물Ethyl (alphaR)-alpha-[(methylsulfonyl)oxy]benzenebutanoateHCID 1479447099.6%

반응 단계

Triethylamine (583 mg) was added dropwise to a stirred mixture of ethyl (R)-2-hydroxy-4-phenylbutyrate (1.0 g) and methanesulfonyl chloride (660 mg) in dichloromethane (10 ml) at ice-bath temperature. After 40 minutes, the reaction mixture was partitioned between dichloromethane and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo to give ethyl (R)-2-methylsulfonyloxy-4-phenylbutyrate (1.37 g) as an oil. This material was used immediately without further purification. NaH (60% in mineral oil, 192 mg) was added to a solution of 4-imidazolecarboxamide (534 mg) in DMF (8 ml) at room temperature. The reaction mixture was stirred for 30 minutes. The methanesulfonate prepared above was added and the resulting mixture was stirred for 3 hours at 60° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06359145B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-8533e20906c04d8ca834359ae849788c
출처 메모uspto-grants-2002_03