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HRID 1995679作成日:2026年10月25日

Hydrochloric Acid → HCID 54515227、化合物

https://huagongshe.com/reaction/1995679

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PyridineHCID 1049—
反応物(4-Fluoro-3-phenoxyphenyl)methanolHCID 12874224—
反応物alpha-Cyclopropyl-4-chlorophenylacetyl chlorideHCID 15083505—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物HCID 54515227HCID 5451522784.4%

反応手順

9.4 g (0.043 mol) of 3-phenoxy-4-fluoro-benzyl alcohol and 9.9 g (0.043 mol) of α-cyclopropyl-4-chlorophenyl-acetic acid chloride were dissolved in 100 ml of anhydrous toluene, and 4 g of pyridine, dissolved in 50 ml of anhydrous toluene, were added dropwise at 20°-25° C., while stirring. Stirring was then continued at 25° C. for a further 3 hours. The reaction mixture was poured into 150 ml of water, to which 10 ml of concentrated hydrochloric acid were added, and the organic phase was separated off and washed again with 100 ml of water. The toluene phase was then dried over sodium sulphate and the solvent was distilled off under a waterpump vacuum. Last residues of solvent were removed by brief incipient distillation at a bath temperature of 60° C./1 mm Hg. 14.9 g (84.4% of theory) of α-cyclopropyl-4-chlorophenyl-acetic acid 3-phenoxy-4-fluoro-benzyl ester were obtained as a yellow oil. The structure was confirmed by the H--NMR spectrum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04405639
出典データセットuspto-grants-1983_09
ORD IDord-6843bd4ff5a940648d50483e38644740
出典メモuspto-grants-1983_09