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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707969Generated: November 1, 2026

Pyridine → HCID 15046664, compound

https://huagongshe.com/reaction/1707969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 15046660HCID 15046660—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethanolHCID 887—
ProductHCID 15046664HCID 15046664—

Reaction Steps

A solution of 4.3 g of (S)-3-hydroxy-1-(2-propynyl)-2-pyrrolidinone, 10.6 ml of acetic anhydride, 0.6 ml of pyridine, 0.1 g of 4-(dimethylamino)pyridine and 85 ml of methylene chloride is stirred at room temperature for 18 hours. Twenty-five ml of methyl alcohol is added and the reaction stirred for 20 minutes. The mixture is washed with 1N hydrochloric acid and saturated sodium bicarbonate. The organic layer is dried, passed thorough a pad of hydrous magnesium silicate and concentrated in vacuo to give 4.9 g of the desired product as a pale yellow oil. [α]D26° =+60° (methylene chloride).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356885
Source datasetuspto-grants-1994_10
ORD IDord-ad56d0a41cd1403896f72836d6e38569
Source noteuspto-grants-1994_10