HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 4-(Chloromethyl)-2-methyl-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | 4-(Chloromethyl)-2-methyl-1,3-thiazole | HCID 736341 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Product | 4-(Chloromethyl)-2-methyl-1,3-thiazole | HCID 736341 | — |
| Product | HCID 68446013 | HCID 68446013 | — |
Reaction Steps
According to the description in J. Heterocyclic Chem., 1979, 16, 1563, 4-chloromethyl-2-methylthiazole was synthesized with 1,3-dichloroacetone and thioacetamide as starting materials. The above-obtained 4-chloromethyl-2-methylthiazole was converted to a 4-hydroxymethyl body by dilute sulfuric acid, and then introduced into a 4-formyl body by oxidation of manganese dioxide (yield to this point: 62%). 5-Ethoxycarbonyl-2-methylpyrrolo[3,2-d]thiazole was obtained by making ethyl azidoacetate act on the above product in the presence of sodium ethoxide and further heating in xylene (yield: 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291449B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-a23de3ee6d5646ebb9448c6e78184d51 |
| Source note | uspto-grants-2007_11 |