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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36345Generated: October 25, 2026

Bromobenzene → 4-(1-Oxo-4-methyl-pentyl) bromobenzene

https://huagongshe.com/reaction/36345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantIsocaproic acidHCID 12587—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-(4-Methylpentyl)-phenylethyneHCID 15337560—
Product4-(1-Oxo-4-methyl-pentyl) bromobenzeneHCID 22409079—

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05414007
Source datasetuspto-grants-1995_05
ORD IDord-f287d333fd274c6d841027fe31376c4c
Source noteuspto-grants-1995_05