4-(Bromomethyl)benzyl alcohol → 4-(Bromomethyl)benzaldehyde

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.

1. filtrationThe reaction mixture was then filtered through a CELITE® pad
2. concentrationconcentrated in vacuo
3. custompartitioned between equal volumes of diethyl ether and water
4. washThe organic fraction was washed with water
5. dry with materialwith brine, and dried over magnesium sulfate
6. customThe solvents were removed in vacuo
7. customto yield a white crystalline solid
8. customRecrystallization from hot diethyl ether

ORD record

ord-78a8415408f3494da679ef3f8dba716b

Source dataset

uspto-grants-1998_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05747517