HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(Methoxymethyl)-4-methyl-1,3-thiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 53930828 | HCID 53930828 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Methoxymethyl)-4-methyl-1,3-thiazole-5-carboxylic acid | HCID 20088075 | — |
Reaction Steps
6.7 g of 85% potassium hydroxide in 1130 ml of ethanol are added at room temperature to 22.1 g of 2-methoxymethyl-4-methylthiazole-5-carboxylic acid ethyl ester and the reaction mixture is then heated under reflux for 18 hours. After cooling, the ethanol is evaporated off and the residue is dissolved in 200 ml of water. After stirring with active carbon, the mixture is filtered over Hyflo and the filtrate is acidified with concentrated hydrochloric acid with vigorous stirring. The resulting yellowish crystals are filtered off, washed with water and dried. After recrystallisation from tetrahydrofuran/petroleum ether (30°-45° C.) (=10:1) the yellowish crystals melt at 168°-169.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05393766 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-4b748890776d4c28a94c5b6594464130 |
| Source note | uspto-grants-1995_02 |