HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Thiazolidinecarboxylic acid, 2-ethyl- → HCID 21162278, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Thiazolidinecarboxylic acid, 2-ethyl- | HCID 98344 | — |
| Reactant | Ethanethioic acid, S-(3-chloro-2-methyl-3-oxopropyl) ester | HCID 103458 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 21162278 | HCID 21162278 | — |
Reaction Steps
3-Acetylthio-2-methylpropanoic acid chloride (5.4 g. prepared from 3-acetylthio-2-methylpropanoic acid and thionyl chloride, b.p. 80°) and 2 N sodium hydroxide (15 ml.) are added to a solution of 2-ethyl-4-thiazolidinecarboxylic acid [Z. Naturforschg, 17b, 765 (1962)] (5.2 g.) in normal sodium hydroxide (30 ml.) chilled in an ice-water bath. After three hours stirring at room temperature, the mixture is extracted with ether, the aqueous phase is acidified and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate and concentrated to dryness in vacuo to yield 3-(3-acetylthio-2-methylpropanoyl)-2-ethyl-4-thiazolidinecarboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237129 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-1b98a0b94c7c407a853929a0945e6535 |
| Source note | uspto-grants-1980_12 |