Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112359Generated: November 1, 2026

Acetic Anhydride → HCID 22763844, compound

https://huagongshe.com/reaction/1112359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 22763836HCID 22763836—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22763844HCID 22763844—

Reaction Steps

A mixture of 2.28 g. of 4-(1-isoquinolyl)-piperidin-4-ol, 1 ml. of pyridine, 1 ml. of acetic anhydride and 20 ml. of benzene is stirred for 3 hours at 25°. The crude 1-acetyl-4-(1-isoquinolyl)-piperidin-4-ol obtained after the customary work up is heated under reflux with 0.7 g. of LiAlH4 in 40 ml. of THF for 24 hours, under nitrogen. The mixture is worked up with sodium hydroxide solution and chloroform in the customary manner to give 1-ethyl-4-(1-isoquinolyl)-piperidin-4-ol, m.p. 275°-276°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04122180
Source datasetuspto-grants-1978_10
ORD IDord-2b0b0bfd7d9d40029e77c6635392535a
Source noteuspto-grants-1978_10