HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223704Generated: October 25, 2026
Hydrochloric Acid → (4R)-3-[(2S)-S-Benzoyl-3-mercapto-2-methylpropanoyl]-2-(4-methylphenyl)-4-thiazolidinecarboxylic acid
https://huagongshe.com/reaction/223704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (4R)-2-(4-methylphenyl)-1,3-thiazolidine-4-carboxylic acid | HCID 2825743 | — |
| Reactant | (2S)-3-benzoylthio-2-methylpropionyl chloride | HCID 12878434 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4R)-3-[(2S)-S-Benzoyl-3-mercapto-2-methylpropanoyl]-2-(4-methylphenyl)-4-thiazolidinecarboxylic acid | HCID 12915626 | — |
Reaction Steps
4.5 g of (4R)-2-(4-methylphenyl)-4-thiazolidinecarboxylic acid and 4.3 g of sodium carbonate are dissolved in 25 ml of water and 4.9 g of (2S)-S-benzoyl-3-mercapto-2-methylpropanoyl chloride is added dropwise while stirring under ice-cooling. After the addition, the mixture is stirred under ice-cooling for 1 hour and acidified with dilute hydrochloric acid. The produced oil is extracted with ethyl acetate. The ethyl acetate layer is washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated to dryness in vacuo to give oil. The produced oil is purified by silica gel column chromatography to give the titled compound, yield 4.0 g (48%), mp. 131°-132° C. (ethyl acetatehexane), [α]D26 +117.6° (c=1.0, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04356183 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-c53acea2ba8440c0ac34ecaa4ac442c2 |
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| Source note | uspto-grants-1982_10 |
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