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HRID 727389作成日:2026年10月26日

Acetic Anhydride → HCID 15871313、化合物

https://huagongshe.com/reaction/727389

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物1,1,1-TrimethoxybutaneHCID 123512—
反応物[2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazineHCID 688223—
反応物2,5-DimethylbenzoylacetonitrileHCID 15895264—
反応物1-Cyano-1-(2,5-dimethylbenzoyl)-3-methoxy-1-penteneHCID 53648846—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 15871313HCID 15871313—

反応手順

A solution of 0.52 g (3.0 mmol) of 2,5-dimethylbenzoylacetonitrile, 0.45 g (3.0 mmol) of trimethylorthobutyrate and 0.632 g (0.58 mL, 6.2 mmol) of acetic anhydride in 5.0 mL of ethyl acetate was refluxed overnight and then cooled. The solvents were removed in vacuo and the residues were dissolved in 10 mL of ethanol. One-half of this solution, containing 1.5 mmol of 1-cyano-1-(2,5-dimethylbenzoyl)-3-methoxy-1-pentene was mixed with 0.7 mL (0.51 g, 5.0 mmol) of triethylamine and 0.37 g (1.50 mmol) of 2,6-dichloro-4-trifluoromethylphenylhydrazine and refluxed for 2.5 hours. The reaction mixture was cooled and partitioned between dilute hydrogen chloride and ethyl acetate. The organic phase was washed with water and then dried with brine and with magnesium sulfate. The solvent was evaporated to give an oil which was chromatographed on silica gel by the flash method eluting with 4:1 hexane/ethyl acetate to give the title compound as an amorphous foam. Anal. Calcd. for C22H20ON3CL2F3, 469.0935. Found: 469.0889.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05712303
出典データセットuspto-grants-1998_01
ORD IDord-fbc3da8862f144fd81839583d69cc429
出典メモuspto-grants-1998_01