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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079409Generated: October 30, 2026

Trifluoroacetic acid → HCID 67748307, compound

https://huagongshe.com/reaction/1079409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67748269HCID 67748269—
ProductHCID 67748307HCID 67748307102%

Reaction Steps

Trifluoroacetic acid (25 ml) was added to 1-tert-butyloxycarbonyl-4-(N-acetyl-N-hexylaminophenyloxy)piperidine (12.5 g) with ice-cooling and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated and methylene chloride (50 ml) was added to the residue and the mixture was washed with aqueous saturated solution of sodium bicarbonate. The aqueous layer was extracted with methylene chloride (50 ml×3), the combined organic layer were dried over anhydrous sodium sulfate and the solvent was distilled off to obtain 4-(N-acetyl-N-hexylaminophenyloxy)piperidine (9.7 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580883
Source datasetuspto-grants-1996_12
ORD IDord-7c13e4957769429f9bc8186a5fdfd03d
Source noteuspto-grants-1996_12