HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227008Generated: October 30, 2026
Ethyl chloroformate → HCID 4095742, compound
https://huagongshe.com/reaction/2227008
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1,4-Benzenediamine, N1,N1-diethyl-, hydrochloride (1:1) | HCID 75145 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 4095742 | HCID 4095742 | 73% |
Reaction Steps
Ethyl chloroformate (5.0 mL, 52 mmol) was added to a stirred mixture of N,N-diethyl-p-phenylenediamine hydrochloride (10 g, 50 mmol) and sodium hydrogen carbonate (23.0 g) in dichloromethane (120 mL) at room temperature under nitrogen. After four days at room temperature, the precipitate which had formed was removed by filtration through a pad of celite. The solid residue was washed with dichloromethane and the combined dichloromethane extracts were concentrated to produce a black oil, which was redissolved in dichloromethane (110 mL) and stirred with silica (100 cc) for 30 minutes. The silica was then removed by filtration through celite. The residue was washed with additional dichloromethane (3×30 mL) and the combined dichloromethane extracts were concentrated to give N-ethoxycarbonyl-4-diethylaminoaniline (8.55 g, 73% yield) as a pale gray solid which melted at 31°-33° C. The structure of this compound was confirmed by mass spectroscopy and by 1H and 13C NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05350870 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-78a190634c03482895eb151ed3caa20b |
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| Source note | uspto-grants-1994_09 |
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