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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639201Generated: October 30, 2026

1-Octanol → 2(Octyloxy)methylbromobenzene

https://huagongshe.com/reaction/1639201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-OctanolHCID 957—
Reactant2-Bromobenzyl bromideHCID 76965—
ReactantOctanoic acid, lithium salt (1:1)HCID 23673717—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuran hexane dimethyl formamideHCID 86741340—
Product2(Octyloxy)methylbromobenzeneHCID 14676390—

Reaction Steps

Lithium octanoate, prepared from octanol and n-butyllithium, in a mixture of tetrahydrofuran/hexane dimethyl formamide was condensed with 2-bromobenzyl bromide to yield 2(octyloxy)methylbromobenzene. This material was treated with n-butyllithium in ether/hexane mixture and subsequently treated with paraformaldehyde to yield 2-(octyloxy)methylbenzyl alcohol. This material was then treated with triphenyl phosphonine bromide to yield [[2-[(octyloxy)-methyl]phenyl]methyl]triphenyl phosphonium bromide. Condensation of this material with 7-formyl-3-methyl-2,4,6-octatrienoic acid ethyl ester, as in Example 3, followed by hydrolysis, as in Example 5, gave the (All-E)-3,7-Dimethyl-9-[2-[(octyloxy)-methyl]phenyl]-2,4,6,8-nonatetraenoic acid, mp 120-121° (from dichloro methane/hexane mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04883613
Source datasetuspto-grants-1989_11
ORD IDord-20c465dabaa9425b87a73276be83fc3f
Source noteuspto-grants-1989_11