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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286865Generated: October 31, 2026

Acetic Anhydride → HCID 54559907, compound

https://huagongshe.com/reaction/2286865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
SolventWaterHCID 962—
ProductHCID 54559907HCID 54559907—

Reaction Steps

A mixture of 5-hydroxy-2-nitrobenzaldehyde (4 g.) and acetic anhydride (10 ml.) was heated on a steam bath for 1 hour, then poured into water (100 ml.) and extracted with diethyl ether (3×50 ml.). The extracts were combined and dried, and the solvent was evaporated. The residue of 5-acetoxy-2-nitrobenzaldehyde was dissolved in absolute ethanol (100 ml.), and stirred and ice-cooled while sodium borohydride (1.5 g.) was added in portions. The reaction mixture was stirred at room temperature for 1 hour, then water (100 ml.) was added, and the mixture was extracted with ether (3×70 ml.). The extracts were combined and dried, and the solvent was evaporated to give 5-acetoxy-2-nitrobenzyl alcohol, which was hydrogenated by the general process described in the latter part of Example 13(a) to give the required starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04268510
Source datasetuspto-grants-1981_05
ORD IDord-de71f879cc154ade8b3b41a92f376b3d
Source noteuspto-grants-1981_05