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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379377Generated: October 30, 2026

Benzyl 3-benzyloxy-2-chloro-4-methanesulfonylbenzoate → 3-Benzyloxy-2-chloro-4-methanesulfonylbenzoic acid

https://huagongshe.com/reaction/2379377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 3-benzyloxy-2-chloro-4-methanesulfonylbenzoateHCID 15132921—
ReactantSodium hydrochlorideHCID 23872008—
SolventEthanolHCID 702—
Product3-Benzyloxy-2-chloro-4-methanesulfonylbenzoic acidHCID 1513292250.6%

Reaction Steps

2.5 g of benzyl 3-benzyloxy-2-chloro-4-methanesulfonylbenzoate was put into 50 ml of ethanol, and 25 ml of an aqueous solution containing 1 g of sodium hydrochloride was added thereto. The mixture was stirred at room temperature for 30 minutes. Then, ethanol was distilled off, and water was added to the residue. The mixture was washed with chloroform. The aqueous layer was acidified with concentrated hydrochloric acid and then extracted with chloroform. The extract was dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain a crude product of the above identified compound. The crude product was washed with ethanol-isopropyl ether to obtain 1.0 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE034779
Source datasetuspto-grants-1994_11
ORD IDord-fdd975c1a8a040aababee9cf0b4f47b4
Source noteuspto-grants-1994_11