HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348272Generated: October 30, 2026
Phosphorus oxychloride → 2-(3-Bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole
https://huagongshe.com/reaction/348272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(3-Bromophenyl)-4,5-dimethyloxazole-3-oxide | HCID 4087775 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(3-Bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole | HCID 4087903 | 72% |
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176224B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-6edf0e42f05b4d04a6bc5212d9706a85 |
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| Source note | uspto-grants-2007_02 |
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