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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417032Generated: October 31, 2026

Phosphorus oxychloride → 2-(3-Bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole

https://huagongshe.com/reaction/2417032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-(3-Bromophenyl)-4,5-dimethyloxazole-3-oxideHCID 4087775—
SolventChloroformHCID 6212—
Product2-(3-Bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazoleHCID 408790372%

Reaction Steps

A solution of 2-(3-bromophenyl)-4,5-dimethyloxazole-3-oxide (96.6 g, 0.36 mol) in CHCl3 (0.90 L) was treated dropwise with phosphorous oxychloride (61.1 g, 0.40 mol) allowing the reaction to exotherm and then stirred at reflux for 30 min. The reaction was then cooled to room temperature and washed with water (2×1 L). The combined aqueous washes were back extracted with CH2Cl2 (2×400 mL). The organic layers were dried (MgSO4), and the solvent removed in vacuo to give crude product that was recrystallized from hot hexanes (300 mL), decanting the hot supernate away from a dark oily material. The remaining dark oil was agitated in additional hot hexanes (200 mL) and the combined supernates were cooled to 0° C. to crystallize the product which was isolated by filtration to give 74.2 g (72%) of 2-(3-bromophenyl)-4-(chloromethyl)-5-methyloxazole as a lime-green powder. 1H NMR (300 MHz, d6-DMSO) δ 8.19 (s, 1H), 7.93 (d, J=8.0 Hz, 1H), 7.58 (d, J=8.0 Hz, 1H), 7.35 (t, J=8.0 Hz, 1H), 4.45 (s, 2H), 2.41 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825222B2
Source datasetuspto-grants-2004_11
ORD IDord-e22322bfb1534465909dae9f721b5db7
Source noteuspto-grants-2004_11