HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074497Generated: October 25, 2026
Dimethylformamide → 3-(Benzyloxy)-4-bromophenol
https://huagongshe.com/reaction/1074497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 4-Bromoresorcinol | HCID 81105 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(Benzyloxy)-4-bromophenol | HCID 15670654 | — |
Reaction Steps
To a 0° C. slurry of 1.7 g. (42.5 mmoles) of potassium hydride in 35 ml. of N,N-dimethylformamide was slowly added a solution of 7.22 g. (38.2 mmoles) of 4-bromoresorcinol. The resultant mixture was stirred for 30 minutes and then 4.54 ml. (38.2 mmoles) of benzyl bromide was slowly added. The reaction mixture was stirred 3 hours longer at 0° C. and then added to 200 ml. of cold water and 200 ml. of ether. The ether extract was washed twice with 200 ml. portions of water, dried over magnesium sulfate and evaporated to an oil. The crude oil was purified via column chromatography on 400 g. of silica gel eluted with 25% ether-pentane to yield (in order of elution) 2.2 g. (16%) of 2,4-dibenzyloxybromobenzene, 0.21 g. (2%) of 5-benzyloxy-2-bromophenol and 3.52 g. (33%) of 3-benzyloxy-4-bromophenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04391827 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-141f372405984ad0a05c559974bb377e |
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| Source note | uspto-grants-1983_07 |
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