HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 23347209, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-(Diisopropylamino)ethyl chloride | HCID 7312 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(1-bromonaphthalen-2-yl)acetonitrile | HCID 234377 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23347209 | HCID 23347209 | — |
Reaction Steps
69 Parts of α-(1-bromo-2-naphthyl)acetonitrile is stirred in 150 parts by volume of 50% sodium hydroxide and then 0.7 parts of benzyltriethylammonium chloride is added to the mixture. To this mixture is added slowly a solution of 41.82 parts of 2-chloro-N,N-diisopropylethylamine in 150 parts by volume of methylene chloride and the resulting mixture is stirred at room temperature for about 2 hours. Then, additional quantities of methylene chloride and water are added to the reaction mixture. The organic layer is then separated, dried over anhydrous sodium sulfate and concentrated to give α-(1-bromo-2-naphthyl)-α-[2-(diisopropylamino)ethyl]acetonitrile, as a solid. This compound is represented by the following structural formula ##STR34##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04217306 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-8701bd3674de421b99f7d9784aff6bef |
| Source note | uspto-grants-1980_08 |