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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351359Generated: October 25, 2026

1,1,1-Trimethoxy-2-methylpropane → N-(1-Methoxy-2-methylpropylidene)-3-phenyl-1,2,4-thiadiazole-5-sulfonamide

https://huagongshe.com/reaction/2351359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trimethoxy-2-methylpropaneHCID 40495—
Reactant3-Phenyl-1,2,4-thiadiazole-5-sulfonamideHCID 14183132—
SolventHexaneHCID 8058—
ProductN-(1-Methoxy-2-methylpropylidene)-3-phenyl-1,2,4-thiadiazole-5-sulfonamideHCID 53780129—

Reaction Steps

A mixture of 3 g of 3-phenyl-1,2,4-thiadiazole-5-sulfonamide and and 11 ml of trimethyl orthoisobutyrate was warmed to about 90° using an oil bath. After 2.5 hours, the solution was allowed to cool to room temperature, whereupon a precipitate formed. Hexane (25 ml) was added to complete the precipitation. The solid was collected, washed with hexane and vacuum dried (P2O5) to give 3.34 g of solid, m.p. 123°-124°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873239
Source datasetuspto-grants-1989_10
ORD IDord-15425112a26b407ebfdbc81d724cd90f
Source noteuspto-grants-1989_10