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HRID 440934作成日:2026年10月25日

Triethylamine → 2-(2-Chlorophenyl)ethyl methanesulfonate

https://huagongshe.com/reaction/440934

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o-Chlorophenethylic alcoholHCID 88266—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2-Chlorophenyl)ethyl methanesulfonateHCID 2188808798.3%

反応手順

To a solution of 5.26 mL (40 mMol) 2-(2-chlorophenyl)ethanol and 8.36 mL (60 mMol) triethylamine in 100 mL tetrahydrofuran were added dropwise 3.25 mL (42 mMol) methanesulfonyl chloride with cooling. The reaction mixture was stirred 4 hours at ambient and was then concentrated under reduced pressure. The residue was partitioned between dichloromethane and water. The organic phase was separated and washed sequentially with water and saturated aqueous sodium chloride. The remaining organics were dried over sodium sulfate and concentrated under reduced pressure to give 9.22 gm (98.3%) of the title compound as a yellow oil. The product was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05521197
出典データセットuspto-grants-1996_05
ORD IDord-71731d44936e4ba7b5b4d009fd53129c
出典メモuspto-grants-1996_05