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HRID 41726作成日:2026年10月25日

Potassium Carbonate → (E)-3-(3'-Adamantan-1-yl-4'-propoxycarbonyloxymethoxy-biphenyl-4-yl)acrylic acid tert-butyl ester

https://huagongshe.com/reaction/41726

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Iodomethyl 2-(methyl)ethyl carbonateHCID 11042958—
反応物HCID 86660473HCID 86660473—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(E)-3-(3'-Adamantan-1-yl-4'-propoxycarbonyloxymethoxy-biphenyl-4-yl)acrylic acid tert-butyl esterHCID 67426176—

反応手順

A mixture of (E)-3-(3′-adamantan-1yl-4′-hydroxybiphenyl-4-yl)acrylic acid tert-butyl ester (250 mg, 0.581 mmol) and K2CO3 (241 mg, 1.74 mmol) in water (2.9 ml) was stirred at RT for 30 min. Tetrabutylammonium hydrogen sulfate (197 mg, 0.581 mmol) and DCM (1.4 ml) were then added and the stirring maintained for further 10 min. A solution of carbonic acid iodomethyl ester propyl ester (184 mg, 0.755 mmol) in DCM (1.4 ml) was then added dropwise. The biphasic solution was stirred overnight at RT. After standard work-up and removal of the solvent under reduced pressure, the residue was taken up in Et2O. Tetrabutylammonium iodide was filtered off and the solvent was evaporated. (E)-3-(3′-Adamantan-1-yl-4′-propoxycarbonyloxymethoxy-biphenyl-4-yl)acrylic acid tert-butyl ester was obtained (117 mg, 36%) after purification on silica gel (EtOAc/hexane 12:88).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530517B2
出典データセットuspto-grants-2013_09
ORD IDord-b52aefb45520443ca761841de668ff7c
出典メモuspto-grants-2013_09