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HRID 1595512作成日:2026年10月27日

Triethylamine → 4-(Methylcarbonyloxy)phenethyl methanesulfonate

https://huagongshe.com/reaction/1595512

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Benzeneethanol, 4-(acetyloxy)-HCID 586676—
溶媒DichloromethaneHCID 6344—
生成物4-(Methylcarbonyloxy)phenethyl methanesulfonateHCID 2170498997.2%

反応手順

55 g (0.305 mole) 2-(4-methylcarbonyloxyphenyl)-1-ethanol and 34.4 g (0.341 mole) triethylamine in 300 ml dichloromethane were cooled on an ice bath. 38.5 g (0.336 mole) methanesulfonyl chloride was slowly added. The ice bath was removed and the mixture was stirred for 3 hours at room temperature. Water was added and the phases were separated. The organic phase was washed with saturated sodium hydrogen bicarbonate and brine, dried (magnesium sulfate), filtered and evaporated in vacuo to give 76.6 g (yield 97%) of 4-(methylcarbonyloxy)phenethyl methanesulfonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06288096B1
出典データセットuspto-grants-2001_09
ORD IDord-ebd58084eae847f7b137bb1746131eae
出典メモuspto-grants-2001_09