Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54010생성일: 2026년 10월 25일
Triphenylphosphine → ethyl 2-[4-[((2R)-2-tert-butoxycarbonylamino-1-butyl)oxy]phenyl]-3-(5-cyano-2-benzofuranyl)propionate
https://huagongshe.com/reaction/54010
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| 반응물 | N-Boc-(R)-(+)-2-amino-1-butanol | HCID 11435422 | — |
| 반응물 | Ethyl 3-(5-cyano-2-benzofuranyl)-2-(4-hydroxyphenyl)propionate | HCID 21844506 | — |
| 반응물 | (2R)-2-tert-butoxycarbonyl-amino-1-butanol | HCID 86750019 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | ethyl 2-[4-[((2R)-2-tert-butoxycarbonylamino-1-butyl)oxy]phenyl]-3-(5-cyano-2-benzofuranyl)propionate | HCID 53858426 | 39.7% |
반응 단계
In 300 ml of tetrahydrofuran were dissolved 1.1 g of ethyl 3-(5-cyano-2-benzofuranyl)-2-(4-hydroxyphenyl)propionate, 1.24 g of (2R)-2-tert-butoxycarbonyl-amino-1-butanol and 1.72 g of triphenylphosphine. The thus prepared solution was mixed with 1.14 g of diethyl azodicarboxylate and stirred at room temperature for 18 hours. The resulting solution was further mixed with 0.83 g of (2R)-2-tert-butoxycarbonylamino-1-butanol, 1.2 g of triphenylphosphine and 0.76 g of diethyl azodicarboxylate, and the mixture was stirred at room temperature for 18 hours. After concentrating the thus prepared reaction solution to dryness, the resulting residue was purified by subjecting it to silica gel column chromatography using a toluene/ethyl acetate mixture as a developing solvent, thereby obtaining 660 mg of ethyl 2-[4-[((2R)-2-tert-butoxycarbonylamino-1-butyl)oxy]phenyl]-3-(5-cyano-2-benzofuranyl)propionate in a colorless and oily form.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05620991 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-b543b31626cd4385b8e1afa5b7b392db |
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| 출처 메모 | uspto-grants-1997_04 |
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