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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372666Generated: November 1, 2026

4-Hydroxybenzaldehyde → HCID 13463483, compound

https://huagongshe.com/reaction/2372666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 13463452HCID 13463452—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 13463483HCID 1346348385.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

3.7 g of N,N'-dicyclohexylcarbodiimide were added portionwise at 0° C. while stirring to a solution of 3.4 g of (S)-p-(4-methylhexyloxy)benzoic acid, 1.76 g of p-hydroxybenzaldehyde and 0.15 g of 4-(dimethylamino)-pyridine in 100 ml of dichloromethane. The mixture was stirred at 0° C. for a further 1 hour and at room temperature for 2 hours, then filtered and the filtrate was washed with 2N sodium carbonate solution and then with water, dried over sodium sulphate and concentrated. Chromatography of the residue on 120 g of silica gel with hexane/ethyl acetate (vol. 9:1) gave 4.2 g of pure (S)-p-(4-methylhexyloxy)benzoic acid p-formylphenyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100577
Source datasetuspto-grants-1992_03
ORD IDord-c89a9647897d4938b7eda24e08c133ab
Source noteuspto-grants-1992_03