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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781874Generated: October 29, 2026

3,4-Dihydroxy-5-nitrobenzoic acid → 3,4-Diacetoxy-5-nitrobenzoic acid

https://huagongshe.com/reaction/1781874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dihydroxy-5-nitrobenzoic acidHCID 14450982—
SolventAcetic AnhydrideHCID 7918—
Product3,4-Diacetoxy-5-nitrobenzoic acidHCID 15480740—

Reaction Steps

7.3 g of 3,4-dihydroxy-5-nitrobenzoic acid are treated with 30 ml of acetic anhydride, whereupon the mixture is held at the reflux temperature for 8 hours. The reaction mixture is poured on to ice. The separated precipitate is filtered under suction, washed with water and taken up in methylene chloride. The organic phase is dried over sodium sulfate and evaporated. The residue obtained is recrystallized from methylene chloride/n-hexane in the cold. There is obtained 3,4-diacetoxy-5-nitrobenzoic acid in the form of colorless crystals of m.p. 126°-127°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-ec38551a5786499e8975aaf437861770
Source noteuspto-grants-1997_05