HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074065Generated: October 30, 2026
Triethylamine → ethyl 1-benzyl-1H-imidazole-2-carboxylate
https://huagongshe.com/reaction/2074065
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Benzylimidazole | HCID 77918 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | ethyl 1-benzyl-1H-imidazole-2-carboxylate | HCID 39869052 | — |
Reaction Steps
148 g (936 mmol) of 1-benzyl-1H-imidazole are suspended in 480 ml of acetonitrile and, at −20° C., 120 ml (87.1 g; 860 mmol) of triethylamine are added. Over a period of 15 minutes, 211.2 ml (239 g; 2208 mmol) of ethyl chloroformate are then added dropwise. The reaction mixture is stirred at −20° C. for 10 minutes. After warming to 15 to 20° C., the reaction mixture is stirred for 18 h and then concentrated in vacuo. Water, a saturated sodium chloride solution and a saturated sodium bicarbonate solution are added to the residue, and the mixture is extracted three times with ethyl acetate. The combined organic phases are washed with a saturated sodium chloride solution and, after drying with magnesium sulfate, concentrated in vacuo. The residue is subjected to a fractional distillation under high vacuum (boiling point=173 to 181° C., pressure=1.7 to 1.2 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919489B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-271f70d6d38b412b852fdbb898c72a35 |
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| Source note | uspto-grants-2011_04 |
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