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HRID 53138作成日:2026年10月24日

Hydrochloric Acid → 4,4-Di(4-tolyl)-but-3-enoic acid

https://huagongshe.com/ja/reaction/53138

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Diethyl SuccinateHCID 31249—
反応物4,4'-DimethylbenzophenoneHCID 69148—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物4,4-Di(4-tolyl)-but-3-enoic acidHCID 10106981—

反応手順

To a 500 mL round-bottomed flask equipped with condenser and nitrogen inlet were added 29.7 grams (141 mmol) 4,4'-dimethylbenzophenone and 141 mL t-butanol forming a solution, followed by 17.4 grams (155 mmol) potassium t-butoxide and 29.5 grams (170 mmol) diethyl succinate. The reaction was refluxed for 18 hours, cooled, and acidified with 6N hydrochloric acid, then poured into water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated, and the residue taken up in 200 mL glacial acetic acid. It was then treated with 70 mL 48% hydrobromic acid and refluxed for 36 hours. The reaction was cooled, partitioned between water and ethyl acetate, and the combined organic layers washed with water and brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel using methylene chloride/methanol as eluant to afford the product as low melting solid, 25.0 grams (66%), Rf =0.25 in 5% methanol/methylene chloride on silica gel. This material was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618811
出典データセットuspto-grants-1997_04
ORD IDord-2eea09bb3dec46f7858b5a4bdb0b69e7
出典メモuspto-grants-1997_04