HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminoheptane → 1-sec-heptyl-3-n-hexyl-2-S-ethylisothiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminoheptane | HCID 5603 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hexyl isothiocyanate | HCID 78120 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-sec-heptyl-3-n-hexyl-2-S-ethylisothiourea | HCID 13083466 | — |
Reaction Steps
The equipment, procedure and reactants were the same as in Example 31 with the exception that 10.01 g (0.07 mole) of n-hexylisothiocyanate, 8.05 g (0.07 mole) 2-aminoheptane, 35 ml ethanol 2B, 11.7 g (0.075 mole) ethyl iodide, 200 ml of toluene and a one percent solution sodium hydroxide (0.08 mole) were used as reactants and reagents in the procedure. The reaction produced 19.6 g (98 weight percent of theory yield of a clear liquid having a nD30 of 1.4765. The product was identified as the title product by IR and NMR spectra analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04357351 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-83125b7fc31f4b07bc0367c2d27d4ffe |
| Source note | uspto-grants-1982_11 |