HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2-Methyl-4-(6-carbomethoxyhexyl)-thiazole-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 2-Methyl-4-(6-carbomethoxyhexyl)-5-hydroxymethyl-thiazole | HCID 21406417 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methyl-4-(6-carbomethoxyhexyl)-thiazole-5-carbaldehyde | HCID 21406415 | 77.4% |
Reaction Steps
The solution of 2.8 g of crude 2-methyl-4-(6-carbomethoxyhexyl)-5-hydroxymethyl thiazole (XII, R1 = CH3) in 25 ml of dichloromethane was dropwise added to the solution of 16 g of chromium trioxide-dipyiridine complex in 320 ml of dichloromethane. Stirring of the reaction mixture was continued for 30 minutes, then the reaction mixture was filtered and the filtrate was evaporated in vacuo. After purifying the crude product obtained as evaporation residue, by preparative thin layer chromatography using a silica gel layer as adsorbent and a mixture of 50 % ethyl acetate and 50 % of n-heptane as running solvent, 2.15 g of 2-methyl-4-(6-carbomethoxyhexyl)-thiazole-5-carbaldehyde (XIII, R1 = CH3) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052407 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-fd308d2c45654f12bcfe52db554f5dc1 |
| Source note | uspto-grants-1977_10 |