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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616586Generated: October 31, 2026

Boron tribromide → 5-[5-(5-Chloro-2-hydroxy-phenyl)-oxazol-2-yl]-pentanoic acid methyl ester

https://huagongshe.com/reaction/1616586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant5-[5-(5-Chloro-2-methoxy-phenyl)-oxazol-2-yl]-pentanoic acid methyl esterHCID 59167755—
SolventDichloromethaneHCID 6344—
Product5-[5-(5-Chloro-2-hydroxy-phenyl)-oxazol-2-yl]-pentanoic acid methyl esterHCID 6848789982%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve 5-[5-(5-chloro-2-methoxy-phenyl)-oxazol-2-yl]-pentanoic acid methyl ester (4.174 g, 12.89 mmol) in 50 mL of CH2Cl2 and cool the solution to −78° C. Add boron tribromide (48.9 mL of a 1M solution in CH2Cl2) dropwise to the reaction and allow it to warm to ambient temperature and allow it to stir for 27 hours. Cool the reaction to −78° C. and quench it by adding 100 mL of MeOH dropwise to the reaction mixture. Allow the reaction to warm to ambient temperature and stir for 19 hours. Concentrate the reaction mixture in vacuo. Dissolve the residue in CH2Cl2 and wash it with saturated aqueous NaHCO3 and brine. Dry the organic layer with MgSO4. Filter off the drying agent and concentrate in vacuo to afford a crude residue. Purify the residue using silica gel chromatography eluting with hexanes/ethyl acetate mixtures to afford 3.26 g of the titled product (82%): mass spectrum: m/z=310.09 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765796B2
Source datasetuspto-grants-2014_07
ORD IDord-ff0e0a97ee1b45689f75ea8b81027512
Source noteuspto-grants-2014_07