HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (2-Bromo-4-tert-butyl-5-methoxy-phenyl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1206775-43-0 | HCID 53401457 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Sodium Bisulfite | HCID 23665763 | — |
| Product | (2-Bromo-4-tert-butyl-5-methoxy-phenyl)-methanol | HCID 67070042 | 100% |
Reaction Steps
step b—To a solution of 345 (2.08 g, 10.70 mmol) in CCl4 (75 mL) was added NBS (2.10 g, 11.80 mmol). The reaction was stirred for 15 min then diluted with a cold 10% aqueous NaHSO3. The reaction mixture was extracted with DCM. The organic extract was washed with brine, dried (MgSO4), filtered and concentrated. The residue was taken up in hexanes (80 mL) and then concentrated to afford 2.9 g (100%) of 344a as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273773B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-1e744d1e0f6d4be5a7ac2ddaf8c8ce87 |
| Source note | uspto-grants-2012_09 |