HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(5,5-Dimethylhex-3-yn-1-yl)-N-methyl-1-naphthalenemethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-Methyl-N-naphthylmethylamine | HCID 84474 | — |
| Reactant | 3-Hexyn-1-ol, 5,5-dimethyl- | HCID 10374472 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5,5-Dimethylhex-3-yn-1-yl)-N-methyl-1-naphthalenemethanamine | HCID 128499 | — |
Reaction Steps
To a solution of 540 mg 5,5-dimethyl-3-hexyn-1-ol in dimethylformamide (DMF) are added, at 0° 1.2 ml triethylamine. Then are added, dropwise, with stirring, 0.335 ml methanesulfonylchloride. After 2 hours of stirring at room temperature are added 740 mg N-methyl-1-naphthylmethylamine and the mixture is heated overnight at 80°. The solvent is evaporated in vacuum, the residue distributed between saturated aqueous NaHCO3 solution and ethyl acetate, the organic phase washed, dried and evaporated. The crude residue is chromatographed over silicagel (with toluene/ethylacetate 9/1) and the title compound (Compound 1) obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05030625 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-f67839bcf2ca4157889f5e1502296ebe |
| Source note | uspto-grants-1991_07 |