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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542278Generated: October 26, 2026

2-Bromo-2-phenylacetaldehyde → p-Nitroacetophenone

https://huagongshe.com/reaction/542278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-2-phenylacetaldehydeHCID 10888901—
ReactantBromomethyl-p-nitro-phenyl-ketoneHCID 86741403—
Productp-NitroacetophenoneHCID 748798%

Reaction Steps

One proceeds according to Example 14 but bromomethyl-p-nitro-phenyl-ketone is used as starting material in the place of α-bromo-α-phenyl-acetaldehyde. The reaction mixture is not worked up by the extraction method according to Example 14 but by precipitating the product with 50 ml of water, filtering off the same and washing it three times with 20 ml of water each. Thus 16.1 g of the desired compound are obtained, yield 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04656290
Source datasetuspto-grants-1987_04
ORD IDord-da7cefb13510455987f10dbb2632f5d7
Source noteuspto-grants-1987_04