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HRID 902289作成日:2026年10月25日

2-(2-Methoxy-6-vinylphenoxy)but-3-enyl 4-methylbenzenesulfonate → 8-methoxy-2H-1-benzopyran-2-methanol 4-methylbenzenesulfonate

https://huagongshe.com/reaction/902289

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2-Methoxy-6-vinylphenoxy)but-3-enyl 4-methylbenzenesulfonateHCID 59701586—
触媒Benzylidenebis(tricyclohexylphosphine)dichlororutheniumHCID 11967259—
溶媒DichloromethaneHCID 6344—
生成物8-methoxy-2H-1-benzopyran-2-methanol 4-methylbenzenesulfonateHCID 131726841183.5%

反応手順

A solution of 2-(2-methoxy-6-vinylphenoxy)but-3-enyl 4-methylbenzenesulfonate (4.4 g, 12 mmol) in dichloromethane (100 mL) was treated with benzylidene-bis(tricyclohexylphosphine)dichlororuthenium (0.9 g) at 23° C. with stirring. After 4 hours, the solvent volume was reduced under reduced pressure (to ca. 10 mL) and the solution was pre-adsorbed on silica gel (5 g). Purification by flash chromatography using a solvent gradient of 10 to 20% ethyl acetate in hexane provided 8-methoxy-2H-1-benzopyran-2-methanol 4-methylbenzenesulfonate (4.0 g, 98%) as a dark oil. MS (ESI) m/z 345.0 ([M−H]−).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365095B2
出典データセットuspto-grants-2008_04
ORD IDord-ffe8c4d44d0f4701b79ff7778ac5c435
出典メモuspto-grants-2008_04