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HRID 637322作成日:2026年10月27日

Ethanol → tert.-butyl (1R,trans) 2,2-dimethyl-3-[2-phenoxy-2-ethoxycarbonyl-ethenyl]-cyclopropane-carboxylate

https://huagongshe.com/reaction/637322

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Acetic acid, 2-phenoxy-, ethyl esterHCID 17365—
反応物SodiumHCID 5360545—
反応物Tert-butyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylateHCID 11735753—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物tert.-butyl (1R,trans) 2,2-dimethyl-3-[2-phenoxy-2-ethoxycarbonyl-ethenyl]-cyclopropane-carboxylateHCID 86740519—

反応条件

温度20 °C

反応手順

9.9 g of tert.-butyl 2,2-dimethyl-3-formyl-cyclopropane-carboxylate and 28 g of ethyl phenoxyacetate were added dropwise at 0° C. to a mixture of 0.05 ml of ethanol, 1.25 g of sodium in small pieces and 25 ml of toluene and the solution was stirred at 20° C. for 16 hours. 20 ml of toluene were added thereto and the mixture was stirred for 4 hours and was poured into iced water. The mixture was extracted with methylene chloride and the organic phase was evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with a 7-3 hexane-ethyl acetate mixture to obtain 12.47 g of E or Z isomer of tert.-butyl (1R,trans) 2,2-dimethyl-3-[2-phenoxy-2-ethoxycarbonyl-ethenyl]-cyclopropane-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04556666
出典データセットuspto-grants-1985_12
ORD IDord-805ed1e8cbb24b90a570527abb9e86ae
出典メモuspto-grants-1985_12