HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dichloroacetone → 4-(Chloromethyl)-2-phenyl-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thiobenzamide | HCID 683563 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Chloromethyl)-2-phenyl-1,3-thiazole | HCID 236969 | — |
Reaction Steps
A solution of thiobenzamide (1.37 g, 10 mmol) and 1,3-dichloro-acetone (1.27 g, 10 mmol) in ethanol (25 mL) is warmed to 75° C. and stirred at this temperature for 1 h. The resulting solution is cooled, poured into ice then brought to pH 8 with K2CO3 solution (sat.). This mixture is extracted with ethyl acetate, dried over MgSO4 and concentrated to give the title compound. This product is used without further purification. MS (ESI) 210 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005440B1 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-912f867d2520451da7082637ac34dc85 |
| Source note | uspto-grants-2006_02 |