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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248861Generated: November 3, 2026

Carbon Dioxide → Tebuconazole

https://huagongshe.com/reaction/1248861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium HydroxideHCID 14798—
Reactant2-tert-Butyl-2-(2-(4-chlorophenyl)ethyl)oxiraneHCID 94684—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductTebuconazoleHCID 8610288.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

20.7 g (0.3 mole) of 1,2,4-triazole, 4.15 g (0.103 mole) of sodium hydroxide and 1 ml of water were added to a solution of 71.55 g (0.3 mole) of 2-tert.-butyl-2-(4-chloro-phenyl-ethyl)-oxirane in 125 ml of N-methyl-pyrrolidone at room temperature, with stirring. The reaction mixture was heated at 120° C. for 4 hours, with stirring, during which a dry stream of CO2 -free air was slowly passed through. Thereafter, the mixture was worked up by a procedure in which the solvent was distilled off under reduced pressure and the residue which remained was washed with water and then dried and stirred with 150 ml of benzine. The solid product which deposited was filtered off and dried again. 81.9 g (88.8% of theory) of 1-(4-chloro-phenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-yl-methyl)-pentan-3-ol were obtained in this manner.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04626594
Source datasetuspto-grants-1986_12
ORD IDord-688502b4ee3241429fbecc18dea6894a
Source noteuspto-grants-1986_12