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HRID 483016作成日:2026年10月26日

Benzyl Alcohol → Benzyl mesylate

https://huagongshe.com/reaction/483016

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物DichloromethaneHCID 6344—
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
溶媒WaterHCID 962—
生成物Benzyl mesylateHCID 14875785%

反応条件

温度-5 °C

反応手順

Under nitrogen methylene chloride (1.4 liter), benzyl alcohol (129.6 g., 1.2 moles) and triethylamine (182 g., 1.8 moles) were combined, stirred and cooled to -5° C. in an ice-water-acetone bath. A solution of methanesulfonyl chloride (150 g., 1.31 moles) in 100 ml. of methylene chloride was added over 49 minutes, maintaining the temperature between -5° and 2° C. After stirring for 10 minutes at 0°-2° C., the reaction was diluted with 500 ml. of water, precooled to 5° C. The organic layer was separated, washed 2×500 ml. of cold water, dried over MgSO4, filtered and evaporated in vacuo to yield title product as a light yellow oil [190 g.; 85%, 1H-NMR (CDCl3) delta (ppm): 2.9 (s, 3H), 5.2 (s, 2H), 7.4 (m, 5H); Rf 0.75 (CH2Cl2 )]. This product was refrigerated until used in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04576964
出典データセットuspto-grants-1986_03
ORD IDord-7ebc7b50d9d84716bee3a49feea9645d
出典メモuspto-grants-1986_03