HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182756Generated: October 25, 2026
Acetyl chloride → Methyl 5-acetamido-2-bromobenzoate
https://huagongshe.com/reaction/1182756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 5-amino-2-bromobenzoate | HCID 245495 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-acetamido-2-bromobenzoate | HCID 58891822 | 98% |
Reaction Steps
Methyl 5-amino-2-bromobenzoate (Reference Compound No. 1-(1), 21.0 g, 91.2 mmol) and triethylamine (19.0 mL, 137 mmol) were dissolved in anhydrous dichloromethane (450 mL), acetyl chloride (13.0 mL, 182 mmol) was added dropwise in this order over 30 minutes under ice cooling, and then the mixture was stirred at 0° C. for 2 hours. The reaction mixture was washed with water (200 mL, twice), saturated aqueous sodium hydrogen carbonate solution (200 mL, twice), and saturated brine (200 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was filtered with hexane-ethyl acetate (20:1) to give the titled reference compound (24.2 g) as a pale yellow solid. (Yield 98%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08664221B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-b694dee1a6a34946997d2b32388f7b14 |
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| Source note | uspto-grants-2014_03 |
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