HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenol → HCID 11551054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Product | HCID 11551054 | HCID 11551054 | — |
Reaction Steps
Alkylation of 4-bromophenol with 3-methoxybenzyl chloride accorcing to the procedure described in J. Chenm. Soc, 2431 (1958) gave 4-bromo-2-(3′-methoxybenzyl)phenol. This material was converted to compound 75, mp 97-101.5° C., and compound 76, mp 102-106° C., by the procedure similar to that in Example 18 method B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943189B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-7b613c54fde14d479f84a79cca4f6544 |
| Source note | uspto-grants-2005_09 |