HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867908Generated: October 30, 2026
Salicylaldehyde → 2-(2-Hydroxyphenyl)-N-methyl-1,3-thiazolidine-3-carbothioamide
https://huagongshe.com/reaction/867908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Methyl isothiocyanate | HCID 11167 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Hydroxyphenyl)-N-methyl-1,3-thiazolidine-3-carbothioamide | HCID 13749531 | 31.2% |
Reaction Steps
To a solution of cysteamine hydrochloride (11.3 g) in ethanol (250 ml) is added sodium hydroxide (4.0 g), and the mixture is stirred for 30 minutes under argon gas. A solution of 2-hydroxybenzaldehyde (12.2 g) in ethanol (40 ml) is added to the mixture, and the mixture is refluxed for 4 hours. To the mixture is added methyl isothiocyanate (7.9 g), and the mixture is further refluxed for 4 hours. After distilling off the solvent under reduced pressure, a mixture of water and ethanol is added to the resulting residue, and the insoluble crystals are collected by filtration. The crystals thus obtained are washed with water and ethanol and recrystallized from ethanol to give N-methyl-2-(2-hydroxyphenyl)thiazolidine-3-carbothioamide (7.9 g, yield: 31.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04777178 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-3273182fbd5147bfa9a3a0085a757f01 |
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| Source note | uspto-grants-1988_10 |
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