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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911083Generated: October 27, 2026

Triethylamine → tert-butyl 4-(2-hydroxyethyl)-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/1911083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(1H-Pyrazol-4-yl)ethanolHCID 4293604—
Reactanttert-Butyl carbonateHCID 4613278—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4-(2-hydroxyethyl)-1H-pyrazole-1-carboxylateHCID 54249732—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.10 g (9.81 mmol) 2-(1H-pyrazol-4-yl)-ethanol, 0.20 g (1.64 mmol) 4-dimethylaminopyridine and 1.50 ml (10.3 mmol) triethylamine were placed in 30 ml dichloromethane, the reaction mixture was cooled to 0° C. and 2.20 g (9.88 mmol) tert. butyl carbonate was slowly added. The mixture was stirred for 2 h at ambient temperature and then overnight at ambient temperature. It was diluted with 50 ml dichloromethane and washed with 10% citric acid solution and 15% potassium carbonate solution, the organic phase was dried, filtered and the solvent was eliminated from the filtrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604049B2
Source datasetuspto-grants-2013_12
ORD IDord-9b3773329892419daa3a344396e63300
Source noteuspto-grants-2013_12