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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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Diethyl aluminum chlorideHCID 16686102—
반응물6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl AcetateHCID 54467667—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoateHCID 5426877673.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04375475
출처 데이터셋uspto-grants-1983_03
ORD IDord-70e71b7d612e41a19000ff3c86dc976e
출처 메모uspto-grants-1983_03