HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxybenzyl bromide → HCID 16041758, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxybenzyl bromide | HCID 4067207 | — |
| Reactant | 1-Azabicyclo[2.2.1]hept-4-yl(diphenyl)methanol | HCID 42625856 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 16041758 | HCID 16041758 | 10% |
Reaction Steps
Following the general procedure outlined in Example 1, 1-azabicyclo[2.2.1]hept-4-yl(diphenyl)methanol (29.3 mg, 0.105 mmol) and 3-(bromomethyl)phenyl methyl ether (0.03 mL, 0.21 mmol) in 2 CH3CN/3 CHCl3 (2.5 mL) were reacted to give the desired product (5 mg, 10%). EI-MS m/z 400 (M+) Rt (1.72 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767691B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-0ed449aba8b44cfbb0acba66322ef679 |
| Source note | uspto-grants-2010_08 |