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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185477Generated: October 30, 2026

Trifluoroacetic acid → HCID 22458544, compound

https://huagongshe.com/reaction/2185477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-[4-(benzyloxy)phenoxy]piperidine-1-carboxylateHCID 22458519—
SolventDichloromethaneHCID 6344—
ProductHCID 22458544HCID 2245854498.7%

Reaction Steps

Trifluoroacetic acid (6 mL) was added to a solution of N-tert-butoxycarbonyl-4-(4-benzyloxyphenoxy)piperidine (B, 473 mg) in dichloromethane (12 mL) at room temperature. After stirring at room temperature for 20 hr, the reaction was quenched with saturated sodium hydrogen carbonate. The resulting mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo to give the titled compound (345 mg) as a yellow brown solid, which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399629B1
Source datasetuspto-grants-2002_06
ORD IDord-e0b776c03f5549e2b1f3ad7222ff538d
Source noteuspto-grants-2002_06