HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(2-(p-Nitrobenzyloxycarbonylamino)ethoxy)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Nitrobenzyl chloroformate | HCID 78205 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(2-aminoethoxy)acetic Acid | HCID 11170956 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-(p-Nitrobenzyloxycarbonylamino)ethoxy)acetic acid | HCID 19422424 | 99.2% |
Reaction Steps
With cooling on an ice bath, to 596 mg of 2-(2-aminoethoxy)acetic acid dissolved in 10 ml of water was added an ether solution of 883 mg sodium bicarbonate and 1.29 g p-nitrobenzyloxycarbonyl chloride in dropwise manner. After stirring the reaction solution for 17 hours at room temperature, the resulting aqueous layer was collected, adjusted to acidic with concentrated hydrochloric acid and extracted with ethyl acetate, and the resulting organic layer was washed with water and dried over sodium sulfate, followed by evaporation of the solvent under a reduced pressure to yield 1.48 g of 2-(2-(p-nitrobenzyloxycarbonylamino)ethoxy)acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559224 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-f465f527d76741e7a902e9a2b2ca4341 |
| Source note | uspto-grants-1996_09 |