Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732053Generated: October 30, 2026

Bromotrichloromethane → Methyl 2-(3-chlorophenyl)-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/732053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrichloromethaneHCID 6383—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 43405659HCID 43405659—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(3-chlorophenyl)-1,3-oxazole-4-carboxylateHCID 2168135059%

Reaction Steps

To a solution of 2-(3-chloro-benzoylamino)-3-hydroxy-propionic acid methyl ester (7.2 g, 29.6 mmol) in CH2Cl2 at −20° C. was added dropwise De-oxofluor (7.2 g, 32.6 mmol). After stirring at this temperature for 30 min, BrCCl3 (3.6 g, 18.1 mmol) was added dropwise followed by DBU (2.79 g, 18.1 mmol). The mixture was then stirred at 2-3° C. for 8 h ad then quenched with saturated NaHCO3 followed by extraction with ethyl acetate. The organic extract as then washed with brine and dried over Na2SO4 (anhydrous). Purification was performed by flash column chromatography on silica gel using ethyl acetate in hexanes as eluant to afford 2-(3-chloro-phenyl)-oxazole-4-carboxylic acid methyl ester (4.1 g, 59%) as a yellow solid. 1H NMR (CDCl3) d (ppm): 8.30 (s, 1 H), 8.12 (d, 1 H), 7.98 (dd, 1 H), 7.45 (m, 2 H), 3.96 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-215cdfe04ef64c44911aee21e81a68e3
Source noteuspto-grants-2009_09