HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → tert-butyl 2-(4-bromophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Benzeneacetic acid, 4-bromo- | HCID 74654 | — |
| Product | tert-butyl 2-(4-bromophenyl)acetate | HCID 14775457 | — |
Reaction Steps
To a solution of 4-bromophenylacetic acid (5.00 g, 23.2 mmol) in tBuOAc (75 mL) was added BF3.OEt2 (2.95 mL, 23.2 mmol). The mixture was allowed to stir overnight at room temperature and poured into H2O. The aqueous phase was extracted with EtOAc. The organic phase was washed with sat. aq NaHCO3, dried over anhydrous Na2SO4, and concentrated in vacuo. Purification by flash chromatography on silica gel (0% to 100% EtOAc in hexanes) provided the title compound. 1H NMR (500 MHz, CDCl3): δ 7.48 (d, J=8.0 Hz, 2 H), 7.19 (d, J=8.0 Hz, 2 H), 3.52 (s, 2 H), 1.48 (s, 9 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935713B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-33e8eddae4f44679b6271562d3073c7a |
| Source note | uspto-grants-2011_05 |