HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[1-(Isopropylthio)ethyl]-2-nitrobenzene → 2-[1-(Isopropylthio)ethyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[1-(Isopropylthio)ethyl]-2-nitrobenzene | HCID 57498015 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[1-(Isopropylthio)ethyl]aniline | HCID 57498016 | 87.1% |
Reaction Steps
44 g (0.188 mol) 1-[1-(isopropylthio)ethyl]-2-nitrobenzene (VII-1) are dissolved in 250 ml ethanol, mixed with 3 g Raney nickel and hydrogenated in the autoclave for 6 hours at room temperature with 3 bar of hydrogen. After 6 hours another 3 g Raney nickel are added and hydrogenation is continued for another 16 hours at room temperature with 3 bar hydrogen. The catalyst is then removed by filtration and the solvent removed under vacuum. The crude product is purified by column chromatography (silica gel, 3:1 hexane/methyl t-butyl ether). 32 g (97.3% purity by HPLC, 84.4% theoretical yield) of 2-[1-(isopropylthio)ethyl]aniline are obtained as a yellow oil [logP (pH 2.3)=2.45].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07842710B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-0095de273bdc466eb92f63e88a043a39 |
| Source note | uspto-grants-2010_11 |