HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Methyl-4-(6-carboxyhexyl)-thiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(6-Carbomethoxy hexyl)-thiazole-5-carboxylic acid methylester | HCID 53815881 | — |
| Product | 2-Methyl-4-(6-carboxyhexyl)-thiazole-5-carboxylic acid | HCID 21406423 | — |
Reaction Steps
The solution of 8 g of crude 2-methyl-4-(6-carbomethoxyhexyl)-thiazole-5-carboxylic acid methylester (VIII, R1 = CH3) in 25 ml of ethanol was treated with 40 ml of 2 N sodium hydroxide solution. The reaction mixture was refluxed for 30 minutes, then acidified with 5 N sulphuric acid under ice-cooling. After extracting the aqueous reaction mixture with 3 × 75 ml of ethyl acetate, the extract was dried over sodium sulphate and evaporated in vacuo. The obtained crude product was recrystallized from a mixture of acetone and n-hexane, affording 5.3 g of 2-methyl-4-(6-carboxyhexyl)-thiazole-5-carboxylic acid (IX, R1 = CH3). M.p.: 147-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052407 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-54b3328924ad4d36a0df9c9d99756888 |
| Source note | uspto-grants-1977_10 |