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HRID 487369作成日:2026年10月26日

Imidazole → (-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate

https://huagongshe.com/reaction/487369

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物rel-(1R,2S)-2-PhenylcyclohexanolHCID 102793—
反応物Triisopropylsilyl chlorideHCID 139400—
反応物Benzyloxyacetyl chlorideHCID 177085—
溶媒DimethylformamideHCID 6228—
溶媒PentaneHCID 8003—
生成物(-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetateHCID 1005992195%

反応手順

To obtain 1c(-), a solution of (-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate (851 mg, 3.63 mmol) was prepared through esterification of benzyloxyacetyl chloride with (-)-(1R,2S)-2-phenyl-1-cyclohexanol followed by hydrogenolysis. Then, triisopropylsilyl chloride (840 mg, 4.36 mmol) and imidazole (618 mg, 9.08 mmol) in dimethylformamide (DMF) (1.7 mL) was stirred at room temperature for 12-20 hours. The mixture was poured into pentane (25 mL), and washed with water and brine. The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo. The crude product was subjected to a purification on a short silica gel column using hexane/chloroform (3/1) as the eluant to give pure 1c(-) (1.35 g, 95% yield) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05294737
出典データセットuspto-grants-1994_03
ORD IDord-8c8b239c359f4197a5536012d4027c08
出典メモuspto-grants-1994_03