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HRID 630570作成日:2026年10月27日

4-Bromostyrene → 2-Phenylethyl 2-oxo-2-(4-vinylphenyl)acetate

https://huagongshe.com/reaction/630570

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromostyreneHCID 16263—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
反応物Oxalic acid, di(2-phenylethyl) esterHCID 6421929—
触媒Tert-ButylhydroquinoneHCID 16043—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethylacetate heptaneHCID 21899848—
生成物2-Phenylethyl 2-oxo-2-(4-vinylphenyl)acetateHCID 8948804768.1%

反応手順

A Grignard reagent prepared from freshly distilled 4-bromostyrene (9.45 g, 51.6 mmol) and magnesium (1.31 g, 54.0 mmol) in THF (70 mL) was added dropwise to a stirred solution of bis(2-phenylethyl)oxalate (14.0 g, 46.9 mmol) in THF (120 mL) at −60° C. The mixture was left warming to room temperature, and then poured onto a mixture of ice (200 g) and a saturated solution of NH4Cl (200 mL). Extraction with diethyl ether (500 mL), washing with a saturated solution of NaCl (300 mL, 3×), re-extraction of the aqueous phase with ether, drying of the combined organic phases (Na2SO4), adding of tert-butyl hydroquinone (TBHQ, ca. 0.3 mg), concentrating and drying under vacuum (0.5 mbar, 0.5 h) afforded 19.40 g of the crude compound. Column chromatography (SiO2, heptane/ethyl acetate 98:2), adding of TBHQ (0.2 mg) to the product fractions, concentrating and drying under vacuum gave 8.95 g (68%) of the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315763B2
出典データセットuspto-grants-2016_04
ORD IDord-3655e4b7cb7a4ff4b844b76d4115d399
出典メモuspto-grants-2016_04