HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592138Generated: October 27, 2026
Hydrochloric Acid → 4-Bromo-3-(trifluoromethyl)benzeneacetic acid
https://huagongshe.com/reaction/592138
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-3-(trifluoromethyl)phenylacetonitrile | HCID 45933702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-3-(trifluoromethyl)benzeneacetic acid | HCID 26986360 | — |
Reaction Steps
To a flask containing 2-(4-bromo-3-(trifluoromethyl)phenyl)acetonitrile 46-5 (880 mg, 3.3 mmol) were added water (4.5 mL) and dropwise concentrated sulfuric acid (4.5 mL). The reaction mixture was stirred at 115° C. for 4 hours. After cooled down to room temperature, the reaction mixture was poured into water (100 mL). The resulting solution was neutralized with powder sodium carbonate to pH 12, treated with 1N HCl aqueous solution to pH around 2, and extracted with dichloromethane (50 mL×3). The combined organic layers were washed with brine, dried over Na2SO4 and then taken to dryness by rotary evaporation give 2-(4-bromo-3-(trifluoromethyl)phenyl)acetic acid 46-6 as pale yellow solid. MS m/z 283.1 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238646B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-5959ba8f0d4542dda2f68b97e7da3a57 |
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| Source note | uspto-grants-2016_01 |
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