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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937621Generated: October 30, 2026

Acetic Acid → HCID 22461266, compound

https://huagongshe.com/reaction/1937621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 22461293HCID 22461293—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 22461266HCID 2246126685%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of ethyl 6,6-dimethyl-3-ethyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate (5.4 g, 0.02 mol) and KOH (2.9 g, 0.05 mol) in EtOH (25 mL) and water (7.5 mL) was heated at reflux for 6 h. The mixture was cooled to 60° C., and neutralized by the addition of acetic acid. Water (80 mL) was added and the cream precipitate collected by filtration. The precipitate was washed with EtOH and hexane then dried under vacuum at 50° C. The acid (4 g, 83%) was isolated as a cream solid, and used without further purification. mp>198° C. 1H NMR (360 MHz, d6-DMSO δ 1.00 (6H,s), 1.04 (3H,t,J=7.3 Hz), 2.22 (2H,s), 2.62 (2H,s), 2.98 (2H,q,J=7.3 Hz), 11.72 (1H, br s). C13H17NO3. O.4(H2O) requires: C, 64.39; H, 7.40; N, 5.73%. Found:C, 64.38, H, 7.30; N, 5.70%. MS(ES+) 236 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395766B1
Source datasetuspto-grants-2002_05
ORD IDord-63d2f5c8582f4d6fb24dc80101df807d
Source noteuspto-grants-2002_05