Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487445생성일: 2026년 10월 24일
1,5-Hexadiene → 8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl ester
https://huagongshe.com/ko/reaction/487445
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,5-Hexadiene | HCID 11598 | — |
| 반응물 | Thionyl bromide | HCID 68176 | — |
| 반응물 | 8-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-octanoic acid methyl ester | HCID 21692618 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl ester | HCID 54439367 | — |
반응 단계
To 2.46 g (6.5 mmol) of 8-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-octanoic acid methyl ester in 25 ml of tetrahydrofuran there are added 5.5 ml (46 mmol) of hexa-1,5-diene and then, dropwise at -50°, 2.6 ml (32.5 mmol) of thionyl bromide. The mixture is stirred at from 0° to 5° for 2 hours, poured into 25 ml of ice-cold saturated sodium hydrogen carbonate solution and extracted twice with 20 ml of methylene chloride each time. The organic phase is washed with 10 ml of saturated sodium chloride solution, dried over magnesium sulfate and concentrated to dryness by evaporation. The resulting oil is purified by chromatography on silica gel with hexane/ethyl acetate (3:1). 8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl ester is obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05294734 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-2fe920b95e4f44c59f46378a7a39cec0 |
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| 출처 메모 | uspto-grants-1994_03 |
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