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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231606Generated: October 25, 2026

Water → 1-Acetoxymethylcyclobutanecarboxylic Acid

https://huagongshe.com/reaction/231606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-(hydroxymethyl)cyclobutane-1-carboxylateHCID 15670506—
SolventEthanolHCID 702—
Product1-Acetoxymethylcyclobutanecarboxylic AcidHCID 15670507—

Reaction Steps

Sodium hydroxide pellets (1.48 g, 37 mmol) was added to a stirred mixture of ethyl 1-hydroxymethylcyclobutanecarboxylate (4.14 g, 26.1 mmol), water (4 ml) and 95% ethanol (20 ml). The resulting mixture was stirred at room temperature overnight, then concentrated on a roatry evaporator. The residue was treated with toluene (100 ml). Evaporation of this mixture gave a flaky resiude which was further dried under high vacuum. The final residue was treated with pyridine (25 ml) and acetic anhydride (15 ml). The resulting mixture was stirred at room temperature for 18 hour, then heated on a steam bath for 20 minutes. It was cooled to room temperature, added crushed ice, then slowly treated with concentrated HCl (12N, 30 ml) with vigorous stirring. It was extracted with a mixture of diethyl ether (120 ml) and methylene chloride (40 ml). The extract was washed with water (4×100 ml), dried, filtered and evaporated to yield the desired product as a yellow oil: NMR (CDCl3) δ=1.82-2.7 (9H, m containing a singlet at 2.07δ), 4.40 (2H, s), 11.46 (H, bs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847306
Source datasetuspto-grants-1989_07
ORD IDord-a66db22d9b9e4557b3f549f277a8a227
Source noteuspto-grants-1989_07