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HRID 1948977作成日:2026年10月26日

1,1-Dichloroethane → Fentanyl

https://huagongshe.com/reaction/1948977

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-DichloroethaneHCID 6365—
反応物Propionyl chlorideHCID 62324—
反応物N-phenyl-1-(2-phenylethyl)-4-piperidinamineHCID 88890—
生成物FentanylHCID 3345—

反応手順

A solution of 5.5 parts (w/w) of 4-anilino-N-phenethyl-piperidine preferably 1 to 3 parts in 5 to 15 parts (w/w) of dichloroethane preferably 8 to 12 parts was taken in a two neck round bottom flask fitted with a reflux condenser, pressure equalizing funnel and calcium chloride guard tube. To this stirred solution, 2 to 20 parts 9 w/w) of propionyl chloride preferably 5 to 15 parts was added drop wise through pressure equalizing funnel. After 2 to 6 hrs, preferably 4 to 5 hrs stirring at room temperature, the reaction mixture was washed with 20% sodium hydroxide solution. The washings were extracted with 2×50 parts, preferably 65 to 70 parts dichloroethane. The combined organic phase was dried over sodium sulphate and concentrated to give fentanyl. The crude compound was recrystallised from petroleum ether (60 to 80° C.) to give colourless crystals of pure fentanyl having mp 82 to 83° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08399677B2
出典データセットuspto-grants-2013_03
ORD IDord-766d0799bdea45eeaf2062bd98711cc5
出典メモuspto-grants-2013_03