Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384078Generated: October 30, 2026

Hydrochloric Acid → 2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acid

https://huagongshe.com/reaction/384078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-[3-(3-bromophenyl)oxetan-3-yl]acetateHCID 57969689—
SolventMethanolHCID 887—
Product2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acidHCID 57969737105.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-[3-(3-bromophenyl)oxetan-3-yl]acetate (1.5 g, 4.513 mmol) was dissolved in MeOH (25 mL) and cooled to 0° C. NaOH (9.026 mL of 1M, 9.026 mmol) was added and the reaction allowed to warm to rt overnight. The solvent was removed under reduced pressure and the solution neutralised with 2 eq of HCl (1M soln, 9.026 mL) and extracted with ethyl acetate. The combined organics were washed with brine, dried over MgSO4, filtered and the solvent removed under reduced pressure to give 2-[3-(3-bromophenyl)oxetan-3-yl]acetic acid as a viscous yellow oil (1.287 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367697B2
Source datasetuspto-grants-2013_02
ORD IDord-ff646fd7ec88497889b50a53a5775241
Source noteuspto-grants-2013_02