HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophosgene → HCID 21487065, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N2,N2-Diethylpyridine-2,5-diamine | HCID 11788486 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21487065 | HCID 21487065 | 19.1% |
Reaction Steps
Using procedures similar to those employed in Step A of Example 8, the reaction of i5.9 g (0.096 mole of 5-amino-2-diethylaminopyridine with 22.2 g (0.193 mole) of thiophosgene and 5.0 g (0.036 mole) of potassium carbonate in 50 ml of water and 150 ml of chloroform yielded 3.8 g of (2-diethylaminopyridin-5-yl) isothiocyanate as a solid. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310724 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-7483503acfaa418a8d926c988b1cf750 |
| Source note | uspto-grants-1994_05 |