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HRID 912732作成日:2026年10月27日

Trifluoroacetic acid → 4-(4-Bromophenoxy)piperidine

https://huagongshe.com/reaction/912732

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物1-BOC-4-(4-bromophenoxy)piperidineHCID 46739006—
溶媒DichloromethaneHCID 6344—
生成物4-(4-Bromophenoxy)piperidineHCID 12645566107.2%

反応手順

A solution of 3.5 g (9.83 mmol) of 1,1-dimethylethyl 4-[(4-bromophenyl)oxy]-1-piperidinecarboxylate, prepared in Step 4.1., in 20 ml of dichloromethane is admixed with 10 ml of trifluoroacetic acid and the solution is stirred at ambient temperature for 1 hour. It is evaporated to dryness and then the residue is taken up in 30 ml of toluene, which is evaporated again to dryness. The residue is subsequently washed with pentane and then taken up in a mixture of 60 ml of dichloromethane and 20 ml of 4N aqueous ammonia solution. It is stirred vigorously for 15 minutes and then the organic phase is decanted, dried over sodium sulfate and evaporated to dryness, to give 2.7 g of product in oil form, which is used as it is in the following step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08026258B2
出典データセットuspto-grants-2011_09
ORD IDord-ce2540bae9ad4cf9827075799bfa579d
出典メモuspto-grants-2011_09