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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649112Generated: October 31, 2026

4-Hydroxybenzaldehyde → Benzaldehyde, 4-(acetyloxy)-

https://huagongshe.com/reaction/1649112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantAcetic AnhydrideHCID 7918—
SolventPyridineHCID 1049—
ProductBenzaldehyde, 4-(acetyloxy)-HCID 70144—

Reaction Steps

4-Hydroxybenzaldehyde was acetylated with pyridine and acetic anhydride as in Example 12 to give 4-acetoxybenzaldehyde which was subjected to dehydration condensation with ethylene glycol to give 2-(4-acetoxyphenyl)-1,3-dioxolan. To a solution of 2-4-acetoxyphenyl)-1,3-dioxolan (13 g) in dichloromethane, bis(trimethylsilyl)-5-fluorouracil prepared as in Example 1 from 5-fluorouracil (10 g) was added followed by treating as in Example 10 to give 4.5 g of crystalline 1-[α-(2-hydroxyethoxy)-4-acetoxybenzyl]-5-fluorouracil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415573
Source datasetuspto-grants-1983_11
ORD IDord-6184d64b464649439e33dc6bde3859e1
Source noteuspto-grants-1983_11