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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612741Generated: October 27, 2026

Water → 4-Amino-5-chloro-2-(2-propenyloxy)benzoic acid

https://huagongshe.com/reaction/1612741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-amino-5-chloro-2-hydroxybenzoateHCID 14883223—
SolventDimethylformamideHCID 6228—
Product4-Amino-5-chloro-2-(2-propenyloxy)benzoic acidHCID 11746364—

Reaction Steps

A suspension of 60% sodium hydride/oil dispersion (1.52 g, 38 mmol) in anhydrous dimethylformamide (50 mL) under nitrogen was treated in portions with 4-amino-5-chloro-2-hydroxybenzoic acid methyl ester (6.05 g, 30 mmol), stirred at room temperature for 30 minutes, and treated with allyl bromide (4.60 ,g 38 mmol). The mixture was stirred at 95±5° C. for one hour, cooled to room temperature, and added to water (250 mL). The solid was removed by filtration and saved, and the filtrate was extracted with ether (2×100 mL). The concentrated ethereal extracts were combined with the filtrated solid, taken up in 20% aqueous ethanol (100 mL), treated with potassium hydroxide (10 g), and refluxed for 45 minutes. The ethanol was removed in vacuo and the aqueous solution was extracted with ether (50 mL) and petroleum ethers (30°-60°, 50 mL), cooled (0° C.), and acidified to pH 4 with concentrated hydrochloric acid (17 mL).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190953
Source datasetuspto-grants-1993_03
ORD IDord-6a2ee85c744f4e3bb3800a8db654d738
Source noteuspto-grants-1993_03