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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492014Generated: October 24, 2026

Methanol → ethyl 2-((N-(butyloxycarbonyl)-N-methylsulfamoyl)amino)acetate

https://huagongshe.com/en/reaction/492014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactantethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetateHCID 18449914—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-((N-(butyloxycarbonyl)-N-methylsulfamoyl)amino)acetateHCID 18449912—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methanol (8.5 mmol) and triphenylphosphine (2.6 g, 8.5 mol) in dry THF is added a solution of ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetate from the previous step (2.4 g, 8.5 mol) and DIAD (2.0 g, 8.5 mmol) in dry THF dropwise at 0° C. under N2 atmosphere. The mixture is stirred at 0° C. for 2 h, warmed to RT and is stirred overnight. After the solvent is removed in vacuo, the residue is purified by column chromatography to afford ethyl 2-((N-(butyloxycarbonyl)-N-methylsulfamoyl)amino)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531566B2
Source datasetuspto-grants-2009_05
ORD IDord-cb334018ecbf43fda115944cc9dfa34b
Source noteuspto-grants-2009_05