HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616205Generated: October 29, 2026
Acetic Anhydride → HCID 20370896, compound
https://huagongshe.com/reaction/616205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | [4-Phenyl-1-(3,3,3-triphenylpropyl)piperidin-4-yl]methanol--hydrogen chloride (1/1) | HCID 20370855 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20370896 | HCID 20370896 | — |
Reaction Steps
A mixture of 1.0 part of 1-(3,3,3-triphenylpropyl)-4-phenyl-4-piperidinemethanol hydrochloride, 10 parts by volume of pyridine and 3.0 parts by volume of acetic anhydride is allowed to stand for 24 hours. Volatile material is removed under reduced pressure and the resulting residue is partitioned between dilute sodium hydroxide and ether. The ether layer is separated, washed with water, dried over sodium sulfate and then treated with an excess of a solution of hydrogen chloride in 2-propanol. The solid which forms is separated by filtration and then washed successively with ether, water, and ether, and then air dried to give 1-(3,3,3-triphenylpropyl)-4-phenyl-4-acetoxymethylpiperidine hydrochloride melting at about 211°-213° C and having the following structural formula ##STR19## Replacement of acetic anhydride with 3.0 parts of propionic acid anhydride provides 1-(3,3,3-triphenylpropyl)-4-phenyl-4-propionyloxymethylpiperidine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04072686 |
|---|
| Source dataset | uspto-grants-1978_02 |
|---|
| ORD ID | ord-14de6428217c468dbef21b765b53181d |
|---|
| Source note | uspto-grants-1978_02 |
|---|