HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cysteamine Hydrochloride → 2-{[(Pyridin-4-yl)methyl]sulfanyl}ethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 23313627 | HCID 23313627 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-{[(Pyridin-4-yl)methyl]sulfanyl}ethan-1-amine | HCID 13498704 | — |
Reaction Steps
34.1 g of sodium hydroxide was dissolved in 500 ml of ethanol under an argon atmosphere and 48.6 g of 2-mercaptoethanamine hydrochloride and 35 g of 4-chloromethylpyridine pyridine hydrochloride were added with ice bath cooling. The reaction mixture was allowed to warm to room temperature over 2 hours, was concentrated, diluted with 300 ml of water and was extracted with 3×150 ml of dichloromethane. The combined organic layers were washed with 100 ml of saturated brine, dried over potassium carbonate and were evaporated to a dark oil which was distilled. The fractions bp 120°-130° C./0.1 mm amounted to 30.68 g (85%) of 2-[[(4-pyridyl)methyl]thio]ethanamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04599336 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-0535977a567d475a8169cd00ba652490 |
| Source note | uspto-grants-1986_07 |