HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-((2-Chloro-4-nitrophenoxy)methyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-1-fluoro-4-nitrobenzene | HCID 67688 | — |
| Reactant | 1,3-Thiazol-2-ylmethanol | HCID 2795213 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-((2-Chloro-4-nitrophenoxy)methyl)thiazole | HCID 53401006 | 99.2% |
Reaction Steps
2-(2-Chloro-4-nitro-phenoxymethyl)-thiazole is prepared by adding thiazol-2-yl-methanol (2.74 g, 23.76 mmol) to a slurry of sodium hydride (1.21 g of a 60% dispersion in oil, 30.2 mmol) in DMF (10 ml) at 0° C. After several minutes, 2-chloro-1-fluoro-4-nitro-benzene (3.79 g, 21.60 mmol) is added and the reaction mixture warmed to room temperature. The reaction mixture is stirred at room temperature for 3 h, and 60° C. for 16 h. After cooling to room temperature, the reaction mixture is poured into 200 ml water. The resulting precipitate is collected by filtration, washed with water, and dried in vacuo to give 2-(2-chloro-4-nitro-phenoxymethyl)-thiazole (5.80 g, 99%) which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777032B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-67f5b023283a446ba94788242228c1aa |
| Source note | uspto-grants-2010_08 |