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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271212Generated: November 4, 2026

Hydrochloric Acid → 2-Amino-4-(benzyloxy)benzoic acid

https://huagongshe.com/reaction/1271212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl 2-acetamido-4-(benzyloxy)benzoateHCID 69461669—
SolventEthanolHCID 702—
Product2-Amino-4-(benzyloxy)benzoic acidHCID 2354588498.2%

Reaction Steps

A suspension of 1.87 g (4.98 mmol) of 2-acetylamino-4-benzyloxy-benzoic acid benzyl ester in EtOH (20 ml) was treated with 1N NaOH (20–30 ml) and stirred at 95° C.–130° C. (oil bath temperature) until completion of the reaction according to TLC and NMR analysis (reaction time about 34 h). The reaction mixture was cooled to RT, brought to pH 6 on addition of 1N aqueous HCl, the precipitate that formed was filtered off by suction and dried in a high vacuum to give 1.19 g (91.7%) of the desired 2-amino-4-benzyloxy-benzoic acid as an off-white solid. ISP mass spectrum, m/e: 242.2 (M+1 calculated for C14H13NO3: 242).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205309B2
Source datasetuspto-grants-2007_04
ORD IDord-a470bf6560304c04ba726f6a7f75aa29
Source noteuspto-grants-2007_04