HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N~1~,N~3~-Diphenylpropane-1,3-diimine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-Methylbenzothiazole | HCID 8446 | — |
| Reactant | 3H-Indole, 2,3,3-trimethyl- | HCID 15427 | — |
| Product | N~1~,N~3~-Diphenylpropane-1,3-diimine | HCID 111090 | — |
Reaction Steps
2,3,3-Trimethyl indolenine, methylbenzothiazole, iodomethane, and diidopropane were purchased from Aldrich and used without further purification. Malonaldehyde dianil was synthesized according to literature reports (Glauert, R. H. and Mann, F. G. J. Chem. Soc. (1952) 5012, by the method of Claisen (Ber. (1903) 36, 3664). Dry nitrobenzene was freshly distilled from CaH2. Dry triethylamine was distilled from Na°. DMF was predried with MgSO4, fractionally distilled and stored over molecular sieves. All dry solvents were stored under N2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760201 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-2d8dda8314e14012bd68143b2834bfc2 |
| Source note | uspto-grants-1998_06 |