HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216216Generated: October 30, 2026
Hydrochloric Acid → Ethyl 3-(bromophenyl)acetate
https://huagongshe.com/reaction/216216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (3-Bromophenyl)acetic acid | HCID 74653 | — |
| Product | Ethyl 3-(bromophenyl)acetate | HCID 11470552 | 93.4% |
Reaction Steps
HCl is bubbled through a solution of 3-bromophenyl acetic acid (10.5 g, 46.5 mmol) in EtOH (70 mL) chilled at 0° C. for 5 minutes. The flask is capped and stirred at ambient temperature for 5 hours. The mixture is concentrated. The residue is taken up with water (80 mL) and extracted twice with EtOAc (70 mL). The organic extracts are combined and dried over magnesium sulfate, filtered and concentrated to afford (3-bromo-phenyl)-acetic acid ethyl ester [10.55 g, 93.4%] as an oil, which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193183B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-3ff37ecbdf284611b966ae6c2176dfa9 |
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| Source note | uspto-grants-2012_06 |
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