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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703412Generated: October 31, 2026

Ethanol → 4-Hydroxybenzaldehyde

https://huagongshe.com/reaction/1703412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPhenolHCID 996—
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
Product4-HydroxybenzaldehydeHCID 126—
ProductSalicylaldehydeHCID 6998—

Reaction Steps

Sen et al J. Indian Chem. Soc. 9 173 (1932) state that the use of chloroform in an ethyl alcohol solution in the Reimer-Tiemann reaction increases the yield of aldehyde. However, the only example describing the reaction of phenol with chloroform and sodium hydroxide in aqueous ethyl alcohol shows a combined yield for salicylaldehyde and p-hydroxybenzaldehyde of only 33%, based on the phenol reacted. The proportion of salicylaldehyde to p-hydroxybenzaldehyde in the product is about five to one, the same as for the conventional aqueous reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351962
Source datasetuspto-grants-1982_09
ORD IDord-7fc6fb7987b64c39b04f5870873d42c4
Source noteuspto-grants-1982_09