HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21522957, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Bromoethyldimethylamine | HCID 17864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21522953 | HCID 21522953 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 21522957 | HCID 21522957 | — |
Reaction Steps
To a cooled solution of 2.3g (0.01 mole) of product of Example 2 in 50 ml of anhydrous ethanol 0.48g (0.01 mole) of 50% sodium hydride is added in portions. After the evolution of hydrogen has ceased, 1.5g (0.01 mole) of 2-(dimethylamino) ethyl bromide is added dropwise, and the mixture is refluxed with stirring for 3 hours. The solvent is removed in vacuo, the residue is mixed with 25 ml of water and the mixture extracted with chloroform. The chloroform extract is washed with water, dried (MgSO4), and concd. to give 3-[2-(dimethylamino)ethoxy]-1,1-dichloro-1a, 2,7,7a-tetrahydro[1H]-cyclopropa[b]naphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969392 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-fffa347c895e406aa429923173ee3ed7 |
| Source note | uspto-grants-1976_07 |