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HRID 278461作成日:2026年10月26日

Triethylamine → Ethyl (alphaR)-alpha-[(methylsulfonyl)oxy]benzenebutanoate

https://huagongshe.com/reaction/278461

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 (R)-2-hydroxy-4-phenylbutyrateHCID 2733848—
溶媒DichloromethaneHCID 6344—
生成物Ethyl (alphaR)-alpha-[(methylsulfonyl)oxy]benzenebutanoateHCID 1479447099.6%

反応手順

Triethylamine (583 mg) was added dropwise to a stirred mixture of ethyl (R)-2-hydroxy-4-phenylbutyrate (1.0 g) and methanesulfonyl chloride (660 mg) in dichloromethane (10 ml) at ice-bath temperature. After 40 minutes, the reaction mixture was partitioned between dichloromethane and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo to give ethyl (R)-2-methylsulfonyloxy-4-phenylbutyrate (1.37 g) as an oil. This material was used immediately without further purification. NaH (60% in mineral oil, 192 mg) was added to a solution of 4-imidazolecarboxamide (534 mg) in DMF (8 ml) at room temperature. The reaction mixture was stirred for 30 minutes. The methanesulfonate prepared above was added and the resulting mixture was stirred for 3 hours at 60° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06359145B1
出典データセットuspto-grants-2002_03
ORD IDord-8533e20906c04d8ca834359ae849788c
出典メモuspto-grants-2002_03