HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Butanediol → 4-(2-Fluoro-5-bromobenzyloxy)butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-2-(bromomethyl)-1-fluorobenzene | HCID 13553295 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Fluoro-5-bromobenzyloxy)butanol | HCID 21196162 | — |
Reaction Steps
A solution of 1,4-dihydroxybutane (4.0 ml, 45.13 mmol) in N,N-dimethylformamide (62 ml) was treated with sodium hydride (1.98 g of a 60% solution, 49.63 mmol), and stirred for about 50 minutes at ambient temperature. The resulting mixture was cooled to 0° C. and treated with 2-fluoro-5-bromobenzyl bromide (3.0 g, 11.28 mmol). The reaction mixture was then stirred for four hours at ambient temperature. The reaction was quenched with water. The aqueous fraction was extracted with methylene chloride. The organic fractions were combined, and dried over sodium sulfate. The solvents were removed in vacuo. The desired title intermediate was further purified by high performance liquid chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245761B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-96ffe5c3cac14f118bd24bd99d6196d6 |
| Source note | uspto-grants-2001_06 |