HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631942Generated: October 29, 2026
Perchloric Acid → tert-Butyl 2-bromo-3-phenylpropionate
https://huagongshe.com/reaction/1631942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 2-Bromo-3-phenylpropanoic acid | HCID 167544 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | tert-Butyl acetate | HCID 10908 | — |
| Product | tert-Butyl 2-bromo-3-phenylpropionate | HCID 12158486 | — |
Reaction Steps
A mixture of 10.1 g (44.1 mmol) of 2-bromo-3-phenylpropionic acid in tert-butyl acetate (150 ml) was cooled in an ice/water bath. 0.5 ml of perchloric acid was added, and the reaction solution was stirred at room temperature overnight. The reaction solution was slowly added to a saturated aqueous sodium bicarbonate solution (200 ml) and the organic phase was separated off. The aqueous phase was extracted twice with 60 ml of ethyl acetate each time, the combined organic phases were washed with saturated aqueous sodium bicarbonate solution and dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was purified by chromatography on silica gel (mobile phase gradient 20% acetic acid in cyclohexane). Yield: 6.76 g (54%) of colorless oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791148B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-29049e44ea0d419cafd00e2db3c0a568 |
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| Source note | uspto-grants-2014_07 |
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