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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isobutyric Acid | HCID 6590 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Benzyl 3-{[(alpha-Chloroethoxy)carbonyl]aminomethyl}-5-Methyl-Hexanoate | HCID 21113521 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Benzyl 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-5-Methyl-Hexanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423169B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-7215531b15434df8beee00b176cccbb1 |
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| 출처 메모 | uspto-grants-2008_09 |
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