HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Fluoro-1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-fluoro-3,3,5-trimethylbenzo[c][1,2]oxaborol-1(3H)-ol | HCID 86685095 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 6-Fluoro-1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde | HCID 86685097 | 908.7% |
Reaction Steps
To a solution of 6-fluoro-3,3,5-trimethylbenzo[c][1,2]oxaborol-1(3H)-ol (388 mg, 2 mmol) in CCl4 (60 mL) at rt was added benzoyl peroxide (48.4 mg, 0.2 mmol) followed by NBS (783 mg, 4.4 mmol). The reaction mixture was heated under reflux for 16 h, cooled to rt and treated with Na2CO3. The aqueous layer was acidified with 3 N HCl to pH of 3 and extracted with DCM (60 mL×3). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to give 6-fluoro-1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde (378 mg, 91%) as a pale yellow solid. 1H NMR (500 MHz, CDCl3) δ 10.369 (s, 1H), 7.687 (d, J=5.5 Hz, 1H), 7.409 (d, J=8.0 Hz, 1H), 2.715 (s, 3H), 1.484 (s, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853186B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-57f84abaf0f04eaa99c5ab6f1914b610 |
| Source note | uspto-grants-2014_10 |