HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Isothiocyanate → HCID 21519702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Isothiocyanate | HCID 5971 | — |
| Reactant | 4-tert-Butyl-1,2,3,6-tetrahydropyridine | HCID 21519703 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21519702 | HCID 21519702 | — |
Reaction Steps
In 20 ml. of anhydrous tetrahydrofuran there is dissolved 5.0 grams of 4-t-butyl-1,2,3,6-tetrahydropyridine, and with stirring there is added 3.5 grams of allylisothiocyanate in 10 ml of anhydrous tetrahydrofuran. The reaction mixture is stirred for 24 hours at room temperature and the tetrahydrofuran is evaporated in vacuo. The resulting solid is dried at 50°C/20 mmHg. to remove any unreacted allylisothiocyanate to give N-allyl-4-t-butyl-1,2,3,6- -tetrahydro-1-pyridinethiocarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03974283 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-156cd34da4c54483b673ae5ca938c41d |
| Source note | uspto-grants-1976_08 |