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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(1H-Pyrazol-4-yl)ethanol | HCID 4293604 | — |
| Reactant | tert-Butyl carbonate | HCID 4613278 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl 4-(2-hydroxyethyl)-1H-pyrazole-1-carboxylate | HCID 54249732 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604049B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-9b3773329892419daa3a344396e63300 |
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| Source note | uspto-grants-2013_12 |
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