HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 22450976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromoheptane | HCID 12369 | — |
| Reactant | HCID 22450971 | HCID 22450971 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 22450976 | HCID 22450976 | — |
Reaction Steps
is obtained by reacting 2,3-difluoro-4-ethoxythiophenol (obtainable analogously to Reference 7 from 2,3-difluoro-4-ethoxyaniline [189751-13-1]) and 4-hexylphenacyl bromide analogously to Reference 5 to give 6,7-difluoro-2-(4-hexylphenyl)-5-ethoxybenzo[b]thiophene, ether cleavage by means of hydrobromic acid/acetic acid to give 6,7-difluoro-2-(4-hexylphenyl)-5-hydroxybenzo[b]thiophene and Williamson ether synthesis using heptyl 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-b7b10fb1f30f416c9e165ccdb5a6f1e0 |
| Source note | uspto-grants-2002_06 |