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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250559Generated: October 31, 2026

Benzyl chloroformate → Methyl 4-({[(benzyloxy)carbonyl]amino}sulfonyl)benzoate

https://huagongshe.com/reaction/2250559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-sulphamoylbenzoateHCID 89847—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 4-({[(benzyloxy)carbonyl]amino}sulfonyl)benzoateHCID 5744453140.8%

Reaction Steps

A mixture of methyl 4-(aminosulfonyl)benzoate (5.10 g) and potassium carbonate (655 g) in dimethoxyethane (50 mL) was refluxed for 5 minutes. After cooling the mixture, a solution of benzyl chloridocarbonate (5.25 g) in dimethoxyethane (30 mL), and the resulting mixture was refluxed for 1 hour. The reaction was quenched by adding 1N hydrochloric acid (100 mL). The mixture was extracted with ethyl acetate (200 mL), and the organic layer was washed with brine, dried over magnesium sulfate, and evaporated to give a pale yellow oil, which was solidified upon standing. The solid was triturated in diisopropyl ether (30 mL) to give methyl 4-({[(benzyloxy)carbonyl]amino}sulfonyl)benzoate as a white powder (3.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-3ff8e803fed646429f215a08aa3f1fdd
Source noteuspto-grants-2008_01