HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 4-[Hydroxy(di-2-thienyl)methyl]-1-(2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | 1-Azabicyclo[2.2.2]oct-4-yl(di-2-thienyl)methanol | HCID 68865599 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-[Hydroxy(di-2-thienyl)methyl]-1-(2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide | HCID 11641678 | 48.9% |
Reaction Steps
Following the general procedure outlined in Example 4, 1-azabicyclo[2.2.2]oct-4-yl(di-2-thienyl)methanol (0.0658 g, 0.215 mmol) and (2-bromoethyl)benzene (0.050 mL, 0.366 mmol) in 1MeOH/1 CHCl3 (4.0 mL) were reacted to give the desired product (0.0514 g, 48.9%). EI-MS m/z 410 (M+) Rt (1.83 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045469B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-956a842bfd2a454d8586322b2e34aa76 |
| Source note | uspto-grants-2015_06 |