Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Chloromethyl)-2-methyl-1,3-thiazole | HCID 736341 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 23042161 | HCID 23042161 | — |
Reaction Steps
A solution of 8.83 g of 4-phenoxyphenol in 15 ml of absolute dimethylformamide is dripped into 1.5 g of 80% strength sodium hydride in 15 ml of absolute dimethylformamide. Upon completion of hydrogen evolution, 7.0 g of 4-chloromethyl-2-methylthiazole is dripped in and the mixture stirred for 3 hours at 80° C. After the solvent has been removed, the residue is slurried with 200 ml of water and extracted 3 times, each time with 50 ml of ether. After drying over sodium sulfate and removal of the solvent, the crude product is recrystallized from cyclohexane/methyl tert-butyl ether (20:1). There is obtained 6.5 g of 2-methyl-4-[(phenoxyphenoxy)-methyl]-thiazole; m.p.: 70°-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943584 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-d07dad5aebbc46e68a843dff4c0355e6 |
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| Source note | uspto-grants-1990_07 |
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