HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099314Generated: October 25, 2026
Thiocarbonic acid, anhydrosulphide with methyl thiohypochlorite → 2-(2-Pyridyldithio)ethanol
https://huagongshe.com/reaction/1099314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiocarbonic acid, anhydrosulphide with methyl thiohypochlorite | HCID 123417 | — |
| Reactant | Mercapto-ethanol | HCID 4713212 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Pyridyldithio)ethanol | HCID 3653053 | 114.6% |
Reaction Steps
To a solution of methoxycarbonyl sulfenyl chloride (10 mL, 110 mmol), in dichloromethane (100 mL), cooled to 0° C., was added mercaptoethanol (7.6 mL, 110 mmol), dropwise. The reaction mixture was allowed to stir at 0° C. for 30 min. At this point, a solution of 2-mercaptopyridine (12.2 g, 110 mmol) in dichloromethane (160 mL) was added. The solution was allowed to react at 0° C. for 1 hr and then was allowed to warm to RT for another 1 hr. Solid product was observed to have fallen out of solution. TLC (1:1 Pet Ether/EtOAc) showed that significant product had been formed. The reaction mixture was concentrated to a volume of 125 mL. The mixture was filtered through a Buchner funnel The filter cake was washed with dichloromethane and then dried under vacuum overnight to afford 2-(2-(Pyridin-2-yl)disulfanyl)ethanol (23.6 g), as the HCl salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143415B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-6cdfd58a123b48fdbdbed289133bfe67 |
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| Source note | uspto-grants-2012_03 |
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