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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912732Generated: October 25, 2026

Trifluoroacetic acid → 4-(4-Bromophenoxy)piperidine

https://huagongshe.com/reaction/912732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-BOC-4-(4-bromophenoxy)piperidineHCID 46739006—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromophenoxy)piperidineHCID 12645566107.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026258B2
Source datasetuspto-grants-2011_09
ORD IDord-ce2540bae9ad4cf9827075799bfa579d
Source noteuspto-grants-2011_09