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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30525생성일: 2026년 10월 25일

Isobutyric Acid → Benzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-Hexanoate

https://huagongshe.com/reaction/30525

반응식

참여 물질

역할이름HCID투입량
반응물Isobutyric AcidHCID 6590—
반응물4-MethylmorpholineHCID 7972—
반응물Benzyl 3-{[(alpha-Chloroethoxy)carbonyl]aminomethyl}-5-Methyl-HexanoateHCID 21113521—
용매DichloromethaneHCID 6344—
생성물Benzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-HexanoateHCID 66887904—

반응 단계

A solution of (40) (0.53 g, 1.50 mmol) in isobutyric acid (1 mL) was added to a mixture of isobutyric acid (0.96 mL, 10.8 mmol) and N-methylmorpholine (1.14 mL, 10.4 mmol) at room temperature. The resulting reaction mixture was stirred at room temperature for 48 h. The reaction mixture was diluted with dichloromethane, washed successively with water, 10% aqueous NaHCO3 solution and brine, then dried over anhydrous Na2SO4. After filtration and removal of the solvent in vacuo, the residue was purified by flash chromatography on silica gel, eluting with 5% ethyl acetate in hexane to afford the title compound (41) as a mixture of two diastereomers (400 mg, 66%). 1H—NMR (CDCl3, 400 MHz): δ 0.85 (m, 6H), 1.14 (m, 8H), 1.44 (m, 3H), 1.62 (m, 1H), 2.13 (m, 1H), 2.32 (m, 2H), 2.51 (m, 1H), 3.06 (m, 1H), 3.24 (m, 1H) 4.95 (m, 1H), 5.10 (s, 2H), 6.76 (q, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423169B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-7215531b15434df8beee00b176cccbb1
출처 메모uspto-grants-2008_09