HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 7-(cyanoamino)heptanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Ethyl 7-(carbamoylamino)heptanoate | HCID 21501463 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 7-(cyanoamino)heptanoate | HCID 21501476 | — |
Reaction Steps
To a solution of ethyl 7-ureidoheptanoate (2.1 g., 0.01 mole) in pyridine (10 ml.) is added p-toluenesulfonylchloride (2.0 g., excess). The reaction is stirred at room temperature for two hours, poured into water (100 ml.), then extracted with ether (2 × 100 ml.). The ether is washed with 5% hydrochloric acid (2 × 25 ml.), brine, then dried over sodium sulfate. The solvent is removed in vacuo to give ethyl 7-cyanamidoheptanoate as a light yellow oil, yield 1.7 g. (86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989749 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-9189190da2334e40b7d187da88df09e1 |
| Source note | uspto-grants-1976_11 |