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HRID 528488作成日:2026年10月25日

Imidazole → (Tert-butyl-dimethyl-silanyloxy)-cyclopropyl-acetic acid methyl ester

https://huagongshe.com/reaction/528488

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Methyl cyclopropyl(hydroxy)acetateHCID 11073449—
溶媒DichloromethaneHCID 6344—
生成物(Tert-butyl-dimethyl-silanyloxy)-cyclopropyl-acetic acid methyl esterHCID 86711764—

反応手順

To a solution of cyclopropyl-hydroxy-acetic acid methyl ester (1.00 g, 7.68 mmol) in DCM (9 mL) was added tert-butyldimethylsilyl chloride (1.27 g, 8.45 mmol) and imidazole (628 mg, 9.22 mmol). The reaction mixture was stirred at RT for 65 hours before being quenched with water (10 mL) and 1M HCl (5 mL). The mixture was extracted with ethyl acetate (3×15 mL) and the combined organic phases were washed with 1M HCl (10 mL), brine (10 mL), dried (Na2SO4) then concentrated in vacuo. This gave (tert-Butyl-dimethyl-silanyloxy)-cyclopropyl-acetic acid methyl ester as an amber oil (1.66 g, 88%). 1H NMR (400 MHz, CDCl3): δ 3.81 (1H, d, J=6.33 Hz), 3.74 (3H, s), 1.23-1.13 (1H, m), 0.89 (9H, s), 0.52-0.0.38 (4H, m), 0.06 (3H, s), 0.04 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346817B2
出典データセットuspto-grants-2016_05
ORD IDord-aa50b66a045e434a8d9f13d1feb4dc36
出典メモuspto-grants-2016_05