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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050138Generated: October 30, 2026

4-Hydroxybenzaldehyde → p-(4'-n-Butylbenzoyloxy)benzaldehyde

https://huagongshe.com/reaction/2050138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantBenzeneHCID 241—
ReactantPyridineHCID 1049—
Reactant4-Butylbenzoyl chlorideHCID 120049—
SolventWaterHCID 962—
Productp-(4'-n-Butylbenzoyloxy)benzaldehydeHCID 5231030916%

Reaction Steps

4-n-Butylbenzoyl chloride (39, 2 g, 0.2 m) was added dropwise to a solution of 4-hydroxybenzaldehyde (24.4 g), (0.2 m) anhydrous benzene (320 ml) and dry pyridine (30 ml) with stirring. After completion of addition stirring was continued for 24 hours at room temperature. The resulting reaction mixture was poured into cold water. The organic layer was separated and washed with diluted hydrochloric acid solution, diluted potassium hydroxide solution and water, then dried over anhydrous sodium sulfate. The solvent was evaporated and the residue was crystallized from ethanol to yield p-(4'-n-butylbenzoyloxy)benzaldehyde (26.3 g, 46%) mp 49.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200580
Source datasetuspto-grants-1980_04
ORD IDord-c6211577384749ac87e0967df1217f95
Source noteuspto-grants-1980_04