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HRID 1428368作成日:2026年10月25日

Triethylamine → 1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1428368

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Ethyl 1-(hydroxymethyl)cyclopropane-1-carboxylateHCID 12450336—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl esterHCID 5746661094%

反応条件

温度23 °C

反応手順

Triethylamine (5.57 mL, 40.00 mmol) and methanesulfonyl chloride (2.85 mL, 36.60 mmol) were sequentially added to a stirred solution of ethyl 1-(hydroxymethyl)cyclopropanecarboxylate (4.80 g, 33.30 mmol) in dichloromethane (83 mL) at 23° C. The resulting bright yellow solution was stirred at 23° C. for 20 h. The reaction mixture was diluted with water and extracted with dichloromethane. The combined organic layers were dried (MgSO4), filtered, and concentrated to dryness to give the desired product as a brown oil (6.92 g, 94%): 1H NMR (300 MHz, CDCl3) δ 4.33 (s, 2H), 4.16 (q, J=7 Hz, 2H), 3.08 (s, 3H), 1.43 (dd, J=7, 4 Hz, 2H), 1.26 (t, J=7 Hz, 3H), 1.04 (dd, J=7, 4 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08937083B2
出典データセットuspto-grants-2015_01
ORD IDord-95d3ba03b4304c349d5c61f0598d0543
出典メモuspto-grants-2015_01