HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → N-[6-[4-[(2-Naphthalenyl)oxy]butoxy]hexyl]benzenemethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-[4-[(6-Bromohexyl)oxy]butoxy]naphthalene | HCID 19101831 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | N-[6-[4-[(2-Naphthalenyl)oxy]butoxy]hexyl]benzenemethanamine | HCID 19101826 | 95.6% |
Reaction Steps
2-[4-[(6-Bromohexyl)oxy]butoxy]naphthalene (2.25 g) and benzylamine (3.88 g) were stirred under nitrogen at ca. 125° for 2 h. The solution was diluted with 8% sodium bicarbonate (100 ml) and extracted with diethyl ether (2×100 ml), dried and evaporated in vacuo to give an oil. Purification by FCC eluting with System C (98:2:1) gave the title compound as a yellow oil (2.3 g), t.l.c. (System C 40:10:1) Rf 0.71.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997986 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-8fc11ce2d86c4022bc4cdae2c801e075 |
| Source note | uspto-grants-1991_03 |