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 26). In accordance with this scheme, bromobenzene (Compound 27) is reacted under Friedel Crafts conditions (AlCl3) with the acid chloride (Compound 28) prepared in situ from 4-methyl valeric acid, to yield 4-(1-oxo-4-methyl-pentyl)bromobenzene (Compound 29). Compound 29 is reduced under Wolff-Kishner conditions (KOH, NH2NH2) to yield 4-(4-methylpentyl)bromobenzene (Compound 30). The bromobenzene derivative 30 is converted to the ethyne derivative 26 through the intermediate trimethylsilyl ethyne derivative 31 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 | US05516904 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-ce09a0390f36489ca696bd97c06f31a2 |
| Source note | uspto-grants-1996_05 |