Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 85797117 | HCID 85797117 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86751766 | HCID 86751766 | — |
Reaction Steps
0.50 g (1.66 mol) of ethyl (3-(4-(aminoiminomethyl)phenyl)ureido)acetate in 20 ml of THF is treated with 2.7 ml of 1N NaOH and cooled to 0° C. 0.29 ml (1.99 mmol) of benzyl chloroformate is added to this mixture and it is stirred at room temperature for 2 h. The pH is kept between 9 and 10 using 1N NaOH. The mixture is then treated with 50 ml of water and extracted with ethyl acetate. After drying (MgSO4), the solvent is removed in vacuo and the residue is stirred with ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05703050 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-4bbcf1e6cb29437d9fbe364b006ee98a |
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| Source note | uspto-grants-1997_12 |
|---|