HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 4-(4-Methylpentyl)bromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(1-Oxo-4-methyl-pentyl) bromobenzene | HCID 22409079 | — |
| Product | 4-(4-Methylpentyl)bromobenzene | HCID 22409093 | — |
Reaction Steps
Reaction Scheme 5 discloses a specific synthetic route to 4-(4-methylpentyl)-phenylethyne (Compound 28). In accordance with this scheme, bromobenzene (Compound 29) is reacted under Friedel Crafts conditions (AlCl3) with the acid chloride (Compound 30) prepared in situ from 4-methyl valeric acid, to yield 4-(1-oxo-4-methyl-pentyl) bromobenzene (Compound 31). Compound 31 is reduced under Wolff-Kishner conditions (KOH, NH2NH2) to yield 4-(4-methylpentyl) bromobenzene (Compound 32). The bromobenzene derivative 32 is converted to the ethyne derivative 28 through the intermediate trimethylsilyl ethyne derivative 33 in a manner similar to the conversion described in connection with Reaction Scheme 3. ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05349105 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-2f605a78644a402a862fa26dda77aeea |
| Source note | uspto-grants-1994_09 |