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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282783Generated: October 31, 2026

Benzyl Bromide → HCID 21520110, compound

https://huagongshe.com/reaction/1282783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 21520063HCID 21520063—
SolventSodium BicarbonateHCID 516892—
ProductHCID 21520110HCID 21520110—

Reaction Steps

5-Amino-4-(p-methoxyphenoxy)-3-mercaptobenzoic acid (2 g) is dissolved in 1 N sodium hydrogen carbonate (50 ml), and after addition of benzyl bromide (0.85 ml), the reaction mixture is stirred for 17 hours. After extraction twice with diethyl ether (25 ml), the aqueous layer is adjusted to pH 2 by addition of 4 N hydrochloric acid. The precipitated 5-amino-3-benzylthio-4-(p-methoxyphenoxy)-benzoic acid is collected and recrystallized from aqueous ethanol. After drying in vacuo at 80°C, the compound is obtained with a melting point of 158°-161°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03972886
Source datasetuspto-grants-1976_08
ORD IDord-4b82d8cd9d0049d7b24e65d168b06b41
Source noteuspto-grants-1976_08