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HRID 247792作成日:2026年10月26日

Hydrochloric Acid → 1,1,1Trifluoro-2-octyl 4-(2-fluoro-4-decyloxyphenyloxycarbonyl)biphenyl-4'-carboxylate

https://huagongshe.com/reaction/247792

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-DimethylaminopyridineHCID 21885—
反応物[1,1'-Biphenyl]-4,4'-dicarbonyl dichlorideHCID 75374—
反応物(R)-(+)-1,1,1-Trifluoro-2-octanolHCID 2779099—
反応物2-Fluoro-4-decyloxyphenolHCID 19013894—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物1,1,1Trifluoro-2-octyl 4-(2-fluoro-4-decyloxyphenyloxycarbonyl)biphenyl-4'-carboxylateHCID 19013909—

反応手順

Into methylene chloride (20 ml) were added 4,4'-biphenyldicarboxylic acid chloride (0.5 g), (R)-(+)-1,1,1-trifluoro-2-octanol (0.15 g), triethylamine (0.09 g) and dimethylaminopyridine (0.03 g) and the mixture was left to stand for 8 hours in order to allow a reaction to proceed. Thereto were added 2-fluoro-4-decyloxyphenol (0.22 g) and triethylamine (0.09 g), and the mixture was left to stand for 8 hours in order to allow a reaction to proceed. The product was made acidic with 1N hydrochloric acid and extracted with methylene chloride. The extracted layer was washed with 1N aqueous sodium carbonate solution, water, aqueous sodium chloride solution (saturated) and water, in this order, until it was neutralized. After the product was dried over anhydrous magnesium sulfate, it was distilled under reduced pressure to remove the solvent. A solid product thus obtained was purified by silica-gel column chromatography until the titled compound (0.48 g) was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05207947
出典データセットuspto-grants-1993_05
ORD IDord-0a71e7ba947049b6858dbe02c9b3e5ac
出典メモuspto-grants-1993_05