HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053377Generated: October 30, 2026
Triethylamine → N-[2-(ethoxycarbonyl)butyl]-N-ethoxycarbonylalanine
https://huagongshe.com/reaction/2053377
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | N-[2-(ethoxycarbonyl)butyl]alanine | HCID 86598455 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[2-(ethoxycarbonyl)butyl]-N-ethoxycarbonylalanine | HCID 86598454 | — |
Reaction Steps
To a suspension of N-[2-(ethoxycarbonyl)butyl]alanine (21.7 g, 100 mmol) in acetone (250 mL) was added a solution of triethylamine (27.7 mL, 20.2 g, 200 mmol) in acetone (50 mL) followed by ethyl chloroformate (24.8 mL, 28.2 g, 260 mmol) at 0-5° C. After stirring for 2 h at ambient temperature the solvent was evaporated and the residue was stirred with a mixture of water (200 mL) and concentrated hydrochloric acid (2 mL) for 8 h at ambient temperature. The mixture was extracted with ethyl acetate (200 mL) and the solution in ethyl acetate was extracted with cold aqueous sodium hydroxide solution [prepared from ice (100 g) and aqueous sodium hydroxide solution (1N, 200 mL)]. Concentrated hydrochloric acid (15 mL) was added to the aqueous layer and the mixture was extracted with ethyl acetate (200 mL). After drying and evaporation N-[2-(ethoxycarbonyl)butyl]-N-ethoxycarbonylalanine (23.8 g, 82%) was obtained as a yellow oil which can be used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07326794B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-84ea3a3d547e45d5ab5c532bf1c91f9c |
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| Source note | uspto-grants-2008_02 |
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