HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084367Generated: October 29, 2026
Benzyl Bromide → 4-(Phenylmethoxy)benzenebutanol
https://huagongshe.com/reaction/2084367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 4-(4-Hydroxybutyl)phenol | HCID 13392513 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Phenylmethoxy)benzenebutanol | HCID 15328765 | 73.4% |
Reaction Steps
In an argon atmosphere, dry DMF (115 ml) was added to 4-(4-hydroxybutyl)phenol (9.43 g) and 65% oily sodium hydride (2.4 g), followed by stirring for 15 minutes. Next, under ice cooling and stirring, a solution of benzyl bromide (9.87 g) in dry dimethylformamide (29.5 ml) was added drop by drop, followed by stirring at the same temperature for 2 hours. After ice water and a 1 N solution of potassium hydrogen sulfate were added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline, after which it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure; the residue was purified by silica gel column chromatography to yield the titled compound (10.67 g) as a colorless crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716863B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-9f31a58e6a98460ead37c6d8817eddf6 |
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| Source note | uspto-grants-2004_04 |
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