HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidine → 3-(p-Nitrobenzyloxycarbonyl)aminomethylbenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidine | HCID 13504316 | — |
| Reactant | [3-(Aminomethyl)phenyl]methanol | HCID 21880609 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(p-Nitrobenzyloxycarbonyl)aminomethylbenzyl alcohol | HCID 54053962 | — |
Reaction Steps
To 3-hydroxymethylbenzylamine (1.37 g) in tetrahydrofuran (30 ml), a solution of S-p-nitrobenzyloxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine (6.2 g) in tetrahydrofuran (20 ml) was added at room temperature, followed by stirring for 1 hours. The resulting precipitates were removed by filtration and the filtrate was diluted with ethyl acetate, washed with water, dried over anhydrous sodium sulfate and evaporated in vacuo to give an oily residue which was then crystallized from diethyl etherdichloromethane to give 3-(p-nitrobenzyloxycarbonyl)aminomethylbenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742052 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-7822ed32ed3a4e20ab8061e3bff0feaf |
| Source note | uspto-grants-1988_05 |