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HRID 30493作成日:2026年10月26日

2-Oxobutanoic Acid → 2-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

https://huagongshe.com/reaction/30493

反応式

関与物質

役割名称HCID仕込み量
反応物2-Oxobutanoic AcidHCID 58—
反応物(+)-8-PhenylmentholHCID 577105—
触媒p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒BenzeneHCID 241—
生成物2-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl esterHCID 1108839692.5%

反応手順

A solution of 2.28 g 2-oxobutyric acid (2, 22.11 mmol, 1.3 eq), 4.04 g (−)-8-phenylmenthol (18, 17.02 mmol, 1.0 eq) and 169.9 mg para-toluenesulfonic acid monohydrate (0.884 mmol, 0.52 eq) in 48 mL benzene was heated to reflux for 20 h 35 min. After cooling down to room temperature, the solution was washed twice with 50 mL saturated aqueous sodium hydrogencarbonate solution, and subsequently with 50 mL water and 50 mL brine. The organic phase was dried over 5 g sodium sulfate and was filtered. The filter cake was washed with 10 mL benzene. The organic phase was evaporated to dryness in a rotary evaporator (40° C., 20 mbar) yielding the title compound (4.98 g, 92% by weight) as colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423152B2
出典データセットuspto-grants-2008_09
ORD IDord-e0866e356d694e0da29bc5cae5ef3ed2
出典メモuspto-grants-2008_09