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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260254Generated: November 1, 2026

Sodium Hydroxide → 2-Chloro-3-hydroxy-5-nitro-p-anisaldehyde

https://huagongshe.com/reaction/2260254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-3-formyl-6-methoxy-5-nitrophenyl acetateHCID 14450994—
SolventMethanolHCID 887—
Product2-Chloro-3-hydroxy-5-nitro-p-anisaldehydeHCID 14450995—

Reaction Steps

35.8 g of 2-chloro-3-formyl-6-methoxy-5-nitrophenyl acetate are dissolved in 300 ml of methanol. After adding 145 ml of 1N sodium hydroxide solution the mixture is stirred at 23° for 1 hour. After evaporation of the methanol, the residue is diluted with ice-water, made acid with 2N hydrochloric acid and extracted twice with 400 ml of ethyl acetate each time. The organic phases are washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated. The residue is recrystallized from methylene chloride/petroleum ether. There is obtained 2-chloro-3-hydroxy-5-nitro-p-anisaldehyde of m.p. 130°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05476875
Source datasetuspto-grants-1995_12
ORD IDord-346f798ae61c49f49f4001319557502d
Source noteuspto-grants-1995_12