HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzyloxy)-3-bromobenzene → 1-(3-Benzyloxyphenyl)-2-dimethylaminomethyl-4-phenethyl-cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzyloxy)-3-bromobenzene | HCID 2756638 | — |
| Reactant | 2-Dimethylaminomethyl-4-(phenethyl)-cyclohexanone hydrochloride | HCID 18980416 | — |
| Product | 1-(3-Benzyloxyphenyl)-2-dimethylaminomethyl-4-phenethyl-cyclohexanol | HCID 18980508 | 87% |
Reaction Steps
The base of compound (48) was reacted with 1-bromo-3-benzyloxy-benzene corresponding to the conditions described in Example 1. The base obtained was purified with 6:1 ether/methanol via a silica gel column. Compound (50) was obtained in a yield of 87% theoretical.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05801201 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-1fbe2eb38c164f31991fd090afc5d87e |
| Source note | uspto-grants-1998_09 |