HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Chloromethyl)-2-methyl-1,3-thiazole → (2-Methyl-4-thiazolyl)methyl 2-cyanonicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Chloromethyl)-2-methyl-1,3-thiazole | HCID 736341 | — |
| Reactant | Potassium 2-cyanonicotinate | HCID 23690323 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-Methyl-4-thiazolyl)methyl 2-cyanonicotinate | HCID 14330271 | 41% |
Reaction Steps
A mixture of potassium 2-cyanonicotinate (4.1 g; 0.022 mole), 4-chloromethyl-2-methylthiazole (2.95 g; 0.02 mole) and 18-crown-6-ether (0.13 g; 0.0005 mole) in acetonitrile (50 cc) is brought to reflux for 8 hours. The solvent is then evaporated off and the residue taken up in water and extracted with dichloromethane. After drying, evaporation of the dichloromethane and purification by chromatography on a silica column, Compound 1(2.12 g; 41%; m.p. 93° C.) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04908375 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-cbc78a70f2714379b400ab1d2faa5ff6 |
| Source note | uspto-grants-1990_03 |