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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040642Generated: October 31, 2026

Water → 3-(3-Oxocyclobutyl)propanoic acid

https://huagongshe.com/reaction/2040642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-(3-oxocyclobutyl)propanoateHCID 67775333—
SolventMethanolHCID 887—
Product3-(3-Oxocyclobutyl)propanoic acidHCID 6777535794%

Reaction Steps

A solution of ethyl 3-(3-oxocyclobutyl)propanoate (200 mg, 1.18 mmol) in methanol (4 mL) was treated with water (0.75 mL) and a 2N solution of sodium hydroxide (0.75 mL, 1.41 mmol) and the solution was heated at 55° C. till the starting material was consumed by TLC (25% EA/hept). After 1 h the starting material was found to be consumed. The reaction mixture was cooled to room temperature and concentrated to remove the MeOH. The aqueous phase was diluted with 2 mL H2O and made acidic to pH˜2 with 1N HCl. The solution was saturated with NaCl and extracted with three 10 mL portions of ethyl acetate. The organic phase was dried over Na2SO4, filtered and concentrated to yield the title compound (157 mg, 94%) as a light orange viscous oil that was used as is in the next step: GC purity 63.2% (ret. time, 4.27 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580762B2
Source datasetuspto-grants-2013_11
ORD IDord-7058f0d2bdbf45f3ac8163f280d1e087
Source noteuspto-grants-2013_11