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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704073Generated: October 29, 2026

Sodium Acetate → 3-Acetyl-2-indolizinecarboxylic acid, methyl ester

https://huagongshe.com/reaction/704073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantMethyl indolizine-2-carboxylateHCID 600232—
SolventAcetic AnhydrideHCID 7918—
Product3-Acetyl-2-indolizinecarboxylic acid, methyl esterHCID 1571331099.2%

Reaction Steps

A stirred solution of 2-indolizinecarboxylic acid, methyl ester (91.42 g, 0.522 mole) and anhydrous sodium acetate (42.53 g, 0.52 mole) in acetic anhydride (1.1 L) was refluxed, under anhydrous conditions, for 48 hours. After cooling most of the acetic anhydride was evaporated in vacuo. The resulting residue (150 ml) was cooled in an ice water bath and methanol (140 ml) was added to destroy the remaining acetic anhydride. The resulting mixture was poured into water (1.1 L) and the product was extracted with diethyl ether, three times. The ethereal layer was washed with saturated sodium bicarbonate solution, three times, with water, two times, and was dried over magnesium sulfate. Evaporation of solvent yielded 112 g of crude 3-acetyl-2-indolizinecarboxylic acid, methyl ester which was chromatographed on silica gel (3 kg) using 10% acetone in benzene as eluant, to afford the pure compound (85.5 g). For analysis, the product was recrystallized from a mixture of diethyl ether and petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985560
Source datasetuspto-grants-1991_01
ORD IDord-0beb2aa862cc46a58b5647858ef43758
Source noteuspto-grants-1991_01