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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377914Generated: November 1, 2026

Beta-Propiolactone → HCID 16776070, compound

https://huagongshe.com/reaction/1377914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-PropiolactoneHCID 2365—
Reactant4-HydroxybiphenylHCID 7103—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16776070HCID 1677607032.6%

Reaction Steps

To a solution in THF of 4-phenylphenol (1.86 g, 10.9 mmol) was added potassium tert-butoxide (1.22 g, 10.9 mmol). Neat β-propiolactone (0.68 mL, 10.9 mmol) was added dropwise. The resulting white suspension was stirred overnight at ambient temperature and then was concentrated in vacuo. The residue was partitioned between ethyl acetate and saturated aqueous NaHCO3. The organic phase was discarded and the aqueous phase was acidified and extracted twice with ethyl acetate. The ethyl acetate extracts were combined, dried over MgSO4, filtered, and concentrated in vacuo to give 3-(4-phenylphenoxy)propionic acid (0.86 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665777
Source datasetuspto-grants-1997_09
ORD IDord-840f12bec98e44f286675b3b345ddf21
Source noteuspto-grants-1997_09