HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069119Generated: October 27, 2026
4-(Bromomethyl)benzyl alcohol → 4-(Bromomethyl)benzaldehyde
https://huagongshe.com/reaction/1069119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Bromomethyl)benzyl alcohol | HCID 10330434 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Bromomethyl)benzaldehyde | HCID 11206421 | 57.3% |
Reaction Steps
The 4-bromomethylbenzyl alcohol (9.0 g, 43 mmol) was reduced to the corresponding aldehyde by dissolving the above-synthesized intermediate in methylene chloride and then adding pyridinium chlorochromate (14.1 g, 6.5 mmol). The reaction mixture was then allowed to stir at room temperature under a nitrogen atmosphere for about oone hour. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was then filtered through a CELITE® pad, concentrated in vacuo, and then partitioned between equal volumes of diethyl ether and water. The organic fraction was washed with water, then with brine, and dried over magnesium sulfate. The solvents were removed in vacuo to yield a white crystalline solid. Recrystallization from hot diethyl ether yielded 4.9 grams of 4-(bromomethyl)benzaldehyde as needle-like crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251928B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-3f7c01d5f63d416fa7a062c7a1ce2c39 |
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| Source note | uspto-grants-2001_06 |
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