HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 2-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one | HCID 14913369 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carbonitrile | HCID 67257362 | — |
Reaction Steps
To a stirred and cooled solution of 5,6-dihydro-2-methylbenzo[d]thiazol-7(4H)-one (1.67 g, 10 mmol) and TOSMIC (2.5 g, 13 mmol) in a mixture of DME (25 mL) and absolute ethanol (25 mL) was added solid t-BuOK (2.8 g, 24 mmol) portionwise while keeping the reaction temperature between 5 and 10° C. The resulting mixture was stirred at room temperature for 30 minutes and at 30-45° C. for 30 minutes. The resulting suspension was cooled to room temperature. The precipitate (TosK) was removed by filtration and rinsed with DME. The combined DME solutions were concentrated under reduced pressure to give the crude product, which was purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710245B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-33190a766f104e7a9c9532481b7f2d87 |
| Source note | uspto-grants-2014_04 |