HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 5-tert-butyl-3-(3-methylbut-2-enyl)thiazol-2(3H)-imine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,3-Dimethylbutanal | HCID 76335 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 3-Methylbut-2-en-1-amine hydrochloride | HCID 18326564 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-tert-butyl-3-(3-methylbut-2-enyl)thiazol-2(3H)-imine | HCID 66852417 | — |
Reaction Steps
3,3-Dimethylbutanal (0.95 g, 9.1 mmol), 3-methylbut-2-en-1-amine hydrochloride (1.1 g, 9.1 mmol), and triethylamine (1.3 mL, 9.1 mmol) were mixed in 9 mL of dry MeCN with 2 g of 4 Å (8-12 mesh beads) molecular sieves and stirred for 20 hours at room temperature. The reaction was filtered through Celite and washed with 8 mL of MeCN. KSCN (1.2 g, 12.3 mmol) was added and the mixture warmed to 50° C. Iodine (2.3 g, 9.1 mmol) was added and the reaction stirred at 50° C. for 6 hours. 20% Na2S2O5 was added, stirred for 30 minutes and the organic layer separated, dried with Na2SO4 and the solvent removed. The resulting solid was used without further purification. LC/MS m/z 225.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865753B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-6a91e3958e8345c4a415d1f4e7900dc7 |
| Source note | uspto-grants-2014_10 |