HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (2-Bromo-4-fluoro-5-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-Fluoro-3-methoxyphenyl)methanol | HCID 593590 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-Bromo-4-fluoro-5-methoxyphenyl)methanol | HCID 71237874 | 96% |
Reaction Steps
To a solution of (4-fluoro-3-methoxy-phenyl)-methanol (10.0 g, 64.04 mmol) in MeCN (160 mL) was added a solution of NBS (11.4 g, 64.04 mmol) in MeCN (50 mL) and the resulting mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo and the residue was suspended in diethyl ether (200 mL). Solid material was removed by filtration and washed with further diethyl ether. The filtrate was washed with water (200 mL) and brine (100 mL), dried over MgSO4 and concentrated in vacuo to give the title compound as a white solid (14.4 g) in a 96% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895544B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-95ed5d69fb934c2cab84465c34bbcf83 |
| Source note | uspto-grants-2014_11 |