HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426020Generated: November 1, 2026
Benzyl chloroformate → Ethyl 2-(((benzyloxy)carbonyl)amino)-2-cyanoacetate
https://huagongshe.com/reaction/426020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 2-cyano-2-(hydroxyimino)acetate | HCID 6399078 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-(((benzyloxy)carbonyl)amino)-2-cyanoacetate | HCID 9943163 | 64.3% |
Reaction Steps
To a mixture of ethyl 2-cyano-2-hydroxyiminoacetate (100 g, 0.704 mol) and water (600 ml), were added a saturated aqueous solution of sodium bicarbonate (200 ml) and sodium hydrosulfite (340 g, 1.96 mol) under ice-cooling, and then benzyloxycarbonyl chloride (144 g, 0.848 mol) was added dropwise under ice-cooling. After the addition was completed, the reaction solution was stirred at 20-30° C. for about 4 hours. Completion of the reaction was confirmed using TLC shown below, precipitated crystals were collected by filtration and washed with sprayed water (50 ml×3). The obtained crystals were recrystallized from ethanol (600 ml), filtered and washed with sprayed ethanol (50 ml×3), dried in airflow at 40° C. to give ethyl 2-benzyloxycarbonylamino-2-cyanoacetate (118.7 g, yield 64.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106230B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-a6f02f3d59304e3d83f5a90f165e1bd2 |
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| Source note | uspto-grants-2012_01 |
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