HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoro-4-methoxyaniline → Acetic Acid Mixture with Hydrobromic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoro-4-methoxyaniline | HCID 581110 | — |
| Reactant | 3-Fluoro-4-methoxythiophenol | HCID 2759007 | — |
| Reactant | 4-Hexylphenacyl bromide | HCID 12925264 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Product | 7-Fluoro-2-(4-hexylphenyl)-5-methoxybenzo[b]thiophene | HCID 22450973 | — |
Reaction Steps
7-Fluoro-2-(4-hexylphenyl)-5-octyloxybenzo[b]thiophene is obtained by reacting 3-fluoro-4-methoxythiophenol (obtainable analogously to Reference 7 from 3-fluoro-4-methoxyaniline [366-99-4]) and 4-hexylphenacyl bromide analogously to Reference 5 to give 7-fluoro-2-(4-hexylphenyl)-5-methoxybenzo[b]thiophene, ether cleavage by means of hydrobromic acid/acetic acid to give 7-fluoro-2-(4-hexylphenyl]-5-hydroxybenzo[b]thiophene and Williamson ether synthesis using octyl bromide in 2-butanone in the presence of potassium carbonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403172B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-4dcf3e14f975437dacc25a426cdac808 |
| Source note | uspto-grants-2002_06 |