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HRID 130590作成日:2026年10月27日

Pyridine → (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (E)-3-(3,4-difluorophenyl)-2-propenoate

https://huagongshe.com/reaction/130590

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物(-)-MentholHCID 16666—
反応物(2E)-3-(3,4-Difluorophenyl)-2-propenoyl chlorideHCID 9920680—
溶媒TolueneHCID 1140—
生成物(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (E)-3-(3,4-difluorophenyl)-2-propenoateHCID 10268077—

反応条件

温度65 °C

反応手順

A solution of L-menthol (7.1 kg) in toluene (8.5 kg) was added over a 20 minute period to the solution of (E)-3-(3,4-difluorophenyl)-2-propenoyl chloride (prepared as in Step 2) and pyridine (0.18 kg, 2.28 mol) stirring at 65° C. The reaction mixture was stirred at 65° C. for a further 4 hours and 40 minutes after the addition was complete, then cooled to 25° C. and stirred for a 14 hours. The solution was diluted with toluene (16 kg), washed with 5% aqueous sodium chloride (6.4 kg), then 6% sodium hydrogen carbonate (6.47 kg), then water (6.1 kg). The solution was dried azeotropically by distillation of the solvent (20 L) under reduced pressure. Dimethyl sulfoxide (33.9 kg) was added and the remaining toluene was distilled off under reduced pressure, affording 47.3 kg of a solution of (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (E)-3-(3,4-difluorophenyl)-2-propenoate (approx. 13.3 kg) in dimethyl sulfoxide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381828B2
出典データセットuspto-grants-2008_06
ORD IDord-621b09b53e5044528fb29f1328e9c063
出典メモuspto-grants-2008_06