Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29798Generated: October 25, 2026

Water → Tert-butyl [1,1-dimethyl-3-(5-methyl-3-p-tolyl-[1,2,4]triazol-1-yl)-propyl]-carbamate

https://huagongshe.com/reaction/29798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant5-Methyl-3-(4-methylphenyl)-1H-1,2,4-triazoleHCID 43166776—
Reactanttert-butyl N-(4-chloro-2-methylbutan-2-yl)carbamateHCID 57429079—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthyl AcetateHCID 8857—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductTert-butyl [1,1-dimethyl-3-(5-methyl-3-p-tolyl-[1,2,4]triazol-1-yl)-propyl]-carbamateHCID 69538809—

Reaction Steps

1.35 g (34 mmol, 60%) sodium hydride are added at 0° C. to a solution of 4.87 g (28 mmol) 5-methyl-3-p-tolyl-[1,2,4]triazole in 40 mL of DMPU. The reaction mixture is heated to ambient temperature and then stirred for one hour. 9.35 g (42 mmol) tert-butyl (3-chloro-1,1-dimethyl-propyl)-carbamate and 1.87 g (5 mmol) tetrabutylammonium iodide are added and the mixture is stirred overnight at ambient temperature and then for 2 hours at 80° C. The mixture is combined with water and ethyl acetate, the aqueous phase is separated off and extracted with ethyl acetate. The combined organic phases are washed with water and sodium chloride solution, dried with sodium sulphate and evaporated down. The residue is purified by column chromatography (silica gel; petroleum ether/ethyl acetate=1:1). Oil. Yield: 2.97 g (30%); mass spectroscopy [M+H]+=359.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423036B2
Source datasetuspto-grants-2008_09
ORD IDord-9abc96cf68074ffdb19d2362b2f5e482
Source noteuspto-grants-2008_09