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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032344Generated: November 1, 2026

Hydrochloric Acid → 1-[(Diphenylmethoxy)acetyl]-3-phenylpiperidine

https://huagongshe.com/reaction/1032344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant3-PhenylpiperidineHCID 107207—
Reactant(Diphenylmethoxy) acetyl chlorideHCID 13111194—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-[(Diphenylmethoxy)acetyl]-3-phenylpiperidineHCID 1455632765%

Reaction Steps

A solution of 4.5 g (17.2 mmole) of (diphenylmethoxy) acetyl chloride in 50 cm3 of methylene chloride was added drop-wise at room temperature to a solution of 2.8 g (17.2 mmole) of 3-phenylpiperidine [prepared according to M. Julia et al., Bull. Soc. Chim. Fr. 1968, 987] and 3.5 g (34.4 mmole) of triethylamine in 100 cm3 of methylene chloride. The reaction mixture was heated to reflux for 4 hours; it was allowed to stand overnight and was then poured into a solution of 10 cm3 of concentrated hydrochloric acid in 300 cm3 of water. The mixture was extracted with methylene chloride, washed with water and dried on sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel filtration (eluent, hexaneethyl acetate, 1/1), then by recrystallization from a hexane-ethyl acetate mixture. There was obtained 4.3 g (yield: 65%) of 1-[(diphenylmethoxy)acetyl]-3-phenylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957927
Source datasetuspto-grants-1990_09
ORD IDord-93aaf05872ae490a9d9e9749bfb780d3
Source noteuspto-grants-1990_09