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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660804Generated: October 25, 2026

Hydrochloric Acid → 4-(Benzyloxy)-3-nitrobenzoic acid

https://huagongshe.com/reaction/1660804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 4-benzyloxy-3-nitrobenzoateHCID 289857—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzyloxy)-3-nitrobenzoic acidHCID 1612472595%

Reaction Steps

A solution the crude 4-benzyloxy-3-nitro-benzoic acid methyl ester from the previous step in tetrahydrofurane (150 mL) and MeOH (600 mL) was treated with KOH 3N (152 mL) and stirred at room temperature for 18 hours. The mixture was acidified with HCl 3N. The precipitate thus formed was filtered, washing with MeOH/water 1:1 and dried under vacuum. 4-Benzyloxy-3-nitro-benzoic acid (42 g, 95% over two steps) was obtained as a white solid, which was used crude in the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030308B2
Source datasetuspto-grants-2011_10
ORD IDord-6161a1f249a54a6e83476b70aa6fb3b5
Source noteuspto-grants-2011_10