HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73819Generated: October 26, 2026
Triethylamine → 1-[(3-Furanylcarbonyl)amino]cyclohexanecarboxylic acid methyl ester
https://huagongshe.com/reaction/73819
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Furoic acid | HCID 10268 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Methyl 1-aminocyclohexane-1-carboxylate hydrochloride | HCID 22645079 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[(3-Furanylcarbonyl)amino]cyclohexanecarboxylic acid methyl ester | HCID 32474010 | 91% |
Reaction Steps
105 g (550 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added to a solution of 98.8 g (500 mmol) of 1-aminocyclohexanecarboxylic acid methyl ester hydrochloride, 84.2 g (550 mmol) of 1-hydroxybenzotriazole, 56.0 g (500 mmol) of 3-furancarboxylic acid and 152 g (1.5 mol) of triethylamine in 1000 ml of methylene chloride under ice-cooling. After the mixture was stirred at room temperature overnight, the reaction solution was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, the obtained crystal was washed with diisopropyl ether to obtain 114 g (91%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829209B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-6d982d7dece24f8ba484bd1d7ba0af2b |
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| Source note | uspto-grants-2014_09 |
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