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HRID 354573作成日:2026年10月25日

Ethyl bromoacetate → Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoate

https://huagongshe.com/reaction/354573

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物Diethyl aluminum chlorideHCID 16686102—
反応物6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl AcetateHCID 54467667—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoateHCID 5426877673.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04375475
出典データセットuspto-grants-1983_03
ORD IDord-70e71b7d612e41a19000ff3c86dc976e
出典メモuspto-grants-1983_03