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HRID 36923作成日:2026年10月23日

3',4'-Dimethoxycinnamic acid → 3,4-Dimethoxycinnamoylchloride

https://huagongshe.com/ja/reaction/36923

反応式

関与物質

役割名称HCID仕込み量
反応物3',4'-Dimethoxycinnamic acidHCID 16848—
反応物Oxalyl chlorideHCID 65578—
触媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物3,4-DimethoxycinnamoylchlorideHCID 53399206—

反応手順

To a mixture of 3,4-dimethoxycinnamic acid (540 mg), DMF (2 drops) and tetrahydrofuran (10 ml) was added oxalyl chloride (0.27 ml) dropwise. The mixture was stirred at room temperature for 40 minutes, at the end of which time the solvent was distilled off to give 3,4-dimethoxycinnamoyl chloride. The chloride was dissolved in dichloromethane (10 ml) followed by addition of 3-amino-4-(2-methylphenyl)-7,8-dihydrocyclopenta [g] [1]benzopyran-2(6H)-one (582 mg) and N,N-dimethylaniline (0.25 ml). The mixture was then stirred at room temperature for 20 hours, after which it was washed with water, dried (MgSO4) and distilled to remove the solvent. The residue was chromatographed on silica gel and eluted with benzene-acetone (9:1) to give 3-(3,4-dimethoxycinnamoylamino) -4-(2-methylphenyl)-7,8-dihydrocyclopenta[g] 1benzopyran-2(6H)-one as oil. The oil was crystallized from ethanol-isopropyl ether (648 mg, 67.4%). Recrystallization from acetone gave colorless needles, m.p. 159°-160° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05418239
出典データセットuspto-grants-1995_05
ORD IDord-03af43923d334bb58f46283316bba5de
出典メモuspto-grants-1995_05