戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 974997作成日:2026年10月25日

Hydrochloric Acid → 4-(4-Fluorophenyl)but-3-enoic acid

https://huagongshe.com/reaction/974997

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4-FluorobenzaldehydeHCID 68023—
反応物(2-Carboxyethyl)triphenylphosphonium chlorideHCID 10270534—
反応物Potassium tert-butoxideHCID 23665647—
反応物HCID 178418361HCID 178418361—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Fluorophenyl)but-3-enoic acidHCID 1039738550%

反応手順

74.4 g of 4-fluorobenzaldehyde and 233.6 g of β-carboxyethyl-triphenyl phosphonium chloride were suspended in 700 ml of tetrahydrofuran and these were incubated on ice and stirred. Into this 500 ml tetrahydrofuran solution of 141.4 g of potassium tert-butoxide was added slowly dropwise. 30 minutes after temperature was brought to room temperature and then they were stirred for 10 hours. After adding thereto ice water and cleaning with ether, the hydrogen-ion concentration of water layer was set to pH2 with undiluted hydrochloric acid. Extraction was then made with ethyl acetate. After drying with magnesium sulfate and concentration made under reduced pressure, the solid obtained was recrystallized from hydrous ethanol, and 53.98 g of marked compound (yield: 50%) was obtained as white needle crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05607953
出典データセットuspto-grants-1997_03
ORD IDord-1ed36f677c7944f586fef193ca317de3
出典メモuspto-grants-1997_03