HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028940Generated: October 26, 2026
Oxalyl chloride → 2-Bromo-3-methylbenzoyl chloride
https://huagongshe.com/reaction/1028940
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Bromo-3-methylbenzoic acid | HCID 2735588 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-3-methylbenzoyl chloride | HCID 14174375 | — |
Reaction Steps
A suspension of 2-bromo-3-methylbenzoic acid (2.07 g, 9.63 mmol) in DCM (48.1 mL) was cooled to 0° C. Oxalyl chloride (0.9 mL, 10.14 mmol) was added dropwise via syringe. After addition, the cooling bath was removed and the reaction mixture stirred overnight. The mixture was concentrated in vacuo to remove solvent and excess reagent, affording 2-bromo-3-methylbenzoyl chloride as a cloudy white oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735384B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-83032d37c54a46f5b993f92c72bb64b3 |
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| Source note | uspto-grants-2014_05 |
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