HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693763Generated: October 26, 2026
Butyl bromide → 1-Bromo-4-(butoxymethyl)benzene
https://huagongshe.com/reaction/1693763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-4-(butoxymethyl)benzene | HCID 11402253 | 89% |
Reaction Steps
To a solution of 4-bromobenzyl alcohol (10.0 g, 53.5 mmol) in N,N-dimethylformamide (200 mL) was added sodium hydride (3.08 g, 64.2 mmol, 50% in oil) at 0° C. This mixture was stirred for 5 minutes at 0° C., and 1-bromobutane (7.47 mL, 69.3 mmol) was added thereto at 0° C. This mixture was stirred for 40 minutes at room temperature and then stirred for 25 minutes at 70° C. The reaction solution was partitioned into water and ethyl acetate at 0° C. The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=20:1) to obtain the title compound (11.5 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08158657B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-cd90d115bc934c1ea3256276b3778860 |
|---|
| Source note | uspto-grants-2012_04 |
|---|