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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088808Generated: November 2, 2026

Acetic Anhydride → HCID 22161803, compound

https://huagongshe.com/reaction/1088808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 22161767HCID 22161767—
SolventPyridineHCID 1049—
ProductHCID 22161803HCID 22161803—

Reaction Steps

To a solution of 8-(t-butyldimethylsilyloxymethyl)-4-hydroxymethyl-1-ethyl-1,2,3,4-tetrahydroquinoline (1.98 g) in pyridine (5 ml), acetic anhydride was added dropwise with stirring under ice-cooling and the mixture was stirred for 2 hours at room temperature. Pyridine was distilled off under reduced pressure, and the resultant residue was extracted with dichloromethane. After washing with a saturated aqueous solution of copper sulfate and with water in this order, the mixture was dried and the solvent was distilled off under reduced pressure to give 8-t-butyldimethylsilyloxymethyl-4-acetyloxymethyl-1-ethyl-1,2,3,4-tetrahydroquinoline (2.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963566
Source datasetuspto-grants-1990_10
ORD IDord-eb43a212498e42418b51f5fbf2beee62
Source noteuspto-grants-1990_10