HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → Diethyl 2-(benzyloxycarbonylamino)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Propanedioic acid, 2-amino-, 1,3-diethyl ester | HCID 81272 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Diethyl 2-(benzyloxycarbonylamino)malonate | HCID 259787 | — |
Reaction Steps
To a solution of 2-aminomalonic acid diethyl ester (10.0 g) in dioxane (60 ml) and water (36 ml), potassium hydrogen carbonate (10.4 g) was added. After completion of the effervescence benzylchloroformate (7.4 ml) was added. The mixture was stirred at 23° for 1.5 h then it was concentrated under reduced pressure, taken up with diethyl ether (400 ml) and washed with 5% HCl (50 ml) and brine (50 ml). The organic layer was dried over sodium sulphate and concentrated in vacuo to give the title compound as a colorless oil (13.6 g). T.l.c. EA/CH 1:4 Rf=0.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686449 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-3495b0b06fae41468faa12523be56b97 |
| Source note | uspto-grants-1997_11 |