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HRID 324462作成日:2026年10月26日

5-[2-(3-Ethylphenyl)ethyl]-2-methyloxazole-4-carboxylic acid → 7-Ethyl-9,10-dihydro-2-methyl-4H-benzo[5,6]cyclohepta[1,2-d]oxazol-4-one

https://huagongshe.com/reaction/324462

反応式

関与物質

役割名称HCID仕込み量
反応物5-[2-(3-Ethylphenyl)ethyl]-2-methyloxazole-4-carboxylic acidHCID 22003640—
溶媒Thionyl ChlorideHCID 24386—
生成物7-Ethyl-9,10-dihydro-2-methyl-4H-benzo[5,6]cyclohepta[1,2-d]oxazol-4-oneHCID 22003584—

反応手順

A solution of the product from step (vii) (9.5 g) in thionyl chloride (100 ml) was stirred at room temperature for 4 days. After removal of solvent under reduced pressure, the residue was dissolved in 1,2-dichloroethane (200 ml) and treated with aluminium chloride (23 g). The reaction mixture was heated at reflux for 1 hour and allowed to cool. The resultant suspension was partitioned between 10% hydrochloric acid and dichloromethane. The combined extracts were evaporated, triturated with acetonitrile, and filtered through a plug of celite. Evaporation afforded a residue which was purified by chromatography eluting with 50-100% ethyl acetate in isohexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218376B1
出典データセットuspto-grants-2001_04
ORD IDord-439642bca3914b95b6b9a3dedface89f
出典メモuspto-grants-2001_04