HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 13135252, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Propanoic acid, 2-(4-hydroxyphenoxy)-, ethyl ester | HCID 3017597 | — |
| Reactant | HCID 13135251 | HCID 13135251 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13135252 | HCID 13135252 | — |
Reaction Steps
21 g (0.1 mole) of ethyl 2-(4'-hydroxyphenoxy)propionate were heated under reflux for 1 hour with 16.6 g (0.12 mole) of potassium carbonate in 250 ml of acetonitrile in order to form the salt. After adding 24.9 g (0.1 mole) of 2-methylsulfonyl-5-chlorothiazolo[5,4-b]pyridine, the reaction mixture was heated under reflux for a further 10 hours. The salt constituent was filtered off while hot and the solvent was removed. The residue was distilled in a high vacuum. This gave 33.6 g (89% of theory) of ethyl 2-[4-(5-chlorothiazolo[5,4-b]pyridin-2-yloxy)-phenoxy]-propionate, of boiling point 204°-207° C./0.01 mbar, which crystallized completely after a little time (melting point 60°-62° C.). ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04477276 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-124a3874aa72408cb4eecdb4106904a1 |
| Source note | uspto-grants-1984_10 |