HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → HCID 15790198, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | HCID 13291139 | HCID 13291139 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15790198 | HCID 15790198 | — |
Reaction Steps
A mixture-of 10 g of 2-benzylthio-6-bromopyridine, 70 ml of a 40% ethylamine aqueous solution, and a catalytic amount of cuprous chloride was allowed to react in an autoclave at 180° C. for 4 hours. After completion of the reaction, the reaction mixture was poured into water and extracted with methylene chloride. The extract was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: ethyl acetate/hexane=1/19 by volume) to obtain 5.9 g of 2-benzylthio-6-ethylaminopyridine as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05457084 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-74953918cf52486a9f5418003dc9291f |
| Source note | uspto-grants-1995_10 |