HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perchloric Acid → Tert-butyl 2-bromo-2-phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Bromo(phenyl)acetic acid | HCID 97919 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | tert-Butyl acetate | HCID 10908 | — |
| Product | Tert-butyl 2-bromo-2-phenylacetate | HCID 11000147 | — |
Reaction Steps
A mixture of 7.9 g (44.1 mmol) of bromo-phenylacetic acid in tert-butyl acetate (100 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. Yield: 8.41 g (84%) of colorless oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08791148B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-be87328024834e6b89169a4009a55998 |
| Source note | uspto-grants-2014_07 |