Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354573생성일: 2026년 10월 25일
Ethyl bromoacetate → Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoate
https://huagongshe.com/reaction/354573
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl bromoacetate | HCID 7748 | — |
| 반응물 | Diethyl aluminum chloride | HCID 16686102 | — |
| 반응물 | 6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl Acetate | HCID 54467667 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoate | HCID 54268776 | 73.4% |
반응 단계
A solution of 6-(2,4-dichlorophenyl)-2-oxo-5-hexene-4-yl acetate (1.3 g, 4.3 mmole) and ethyl bromoacetate (0.47 ml, 4.2 mmole) in dry THF (10 ml) was added dropwise to a vigorously stirred slurry of activated zinc dust (490 mg, 7.5 mmole), cuprous bromide (29 mg, 0.2 mmole), diethylaluminum chloride (25% solution in toluene; 1.72 ml, 4.3 mmole) and dry THF (5 ml) under N2 at 20° C. Stirring was continued for 5 hours before quenching with pyridine (3.5 ml). After the addition of water (50 ml) the mixture was extracted with ether (3×80 ml). The combined ether extracts were washed with 1 N HCl (2×25 ml), H2O (2×50 ml) and brine, then dried (MgSO4), filtered and evaporated leaving the crude title compound as a pale yellow oil (1.2 g); pmr (CDCl3) δ1.28 (3 H, t), 1.33 (3H, t), 2.10 (3H, s).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04375475 |
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| 출처 데이터셋 | uspto-grants-1983_03 |
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| ORD ID | ord-70e71b7d612e41a19000ff3c86dc976e |
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| 출처 메모 | uspto-grants-1983_03 |
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