HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446135Generated: November 3, 2026
Benzyl chloroformate → Ethyl 3-benzyloxycarbonyl-3-(ethoxycarbonylmethylamino)propionate
https://huagongshe.com/reaction/1446135
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Ethyl 3-(ethoxycarbonylmethylamino)propionate | HCID 281012 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-benzyloxycarbonyl-3-(ethoxycarbonylmethylamino)propionate | HCID 68545045 | — |
Reaction Steps
0.95 kg of ethyl 3-(ethoxycarbonylmethylamino)propionate (4.68 mol) was dissolved in 2.85 L of ethanol and 2.85 L of water. To this solution, 0.41 kg of sodium bicarbonate (4.91 mol) was added under stirring. Subsequently, 0.84 kg of benzylchloroformate (4.91 mol) was added dropwise at an internal temperature of 28 to 35° C. and the mixture was stirred at an internal temperature of 28 to 35° C. for 2 hours. Ethanol was evaporated under reduced pressure and 9.51 L of ethyl acetate was added. The mixture was then stirred for 5 minutes. The mixture was allowed to stand and the organic layer (top layer) was collected. To this layer, 4.8 L of water was added and the mixture was stirred for 5 minutes. The mixture was allowed to stand again and the organic layer (top layer) was collected. To this layer, 4.8 L of 28% brine was added and the mixture was stirred for 5 minutes. The mixture was allowed to stand again and the organic layer (top layer) was collected. To this layer, 0.57 kg of anhydrous sodium sulfate was added and the mixture was stirred for 1 hour. The solid was separated by filtration and washed with 0.95 L of ethyl acetate. The filtrate and the wash were combined and concentrated under reduced pressure. The resulting product was dried under reduced pressure at an external temperature of 50° C. for 30 minutes. This gave 1.64 kg of a crude product of the title compound as a colorless oil. This product was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07667049B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-77fc8e1322c54e209f3f8f5be44702ea |
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| Source note | uspto-grants-2010_02 |
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