Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21659Generated: October 25, 2026

Methanesulfonyl chloride → HCID 178425305, compound

https://huagongshe.com/reaction/21659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Carboxy-1,2,3-triazoleHCID 140120—
ReactantSodium BicarbonateHCID 516892—
ReactantN'-t-butyl-N'-(3-methylbenzoyl)hydrazineHCID 15452040—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178425305HCID 178425305—

Reaction Steps

1,2,3-triazole-4-carboxylic acid (1.0 g) and triethylamine (0.9 g) were dissolved in 40 ml methylene chloride and cooled in an ice bath. Methanesulfonylchloride (1.0 g) was added dropwise. After addition was complete, the reaction mixture was stirred for 0.5 hours. N'-t-butyl-N'-(3-methylbenzoyl)hydrazine (1.84 g) in 10 ml CH2Cl2 was added dropwise. The resulting mixture was allowed to stand for 14 hours. Aqueous sodium bicarbonate was added. The organic layer was dried over anhydrous magnesium sulfate, filtered and evaporated to give a yellow oil. Chromatography on silica gel using acetone as eluant afforded N'-t-butyl-N-1,2,3-triazole-4-carbonyl-N'-(3-methylbenzoyl)hydrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424333
Source datasetuspto-grants-1995_06
ORD IDord-dffaf8d25a7f4b579f3a263f31bda5e4
Source noteuspto-grants-1995_06