Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733521Generated: October 26, 2026

1-Bromo-3-methylbutane → 15-Methylhexadecyl bromide

https://huagongshe.com/reaction/1733521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methylbutaneHCID 7891—
Reactant1,12-DibromododecaneHCID 18766—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product15-Methylhexadecyl bromideHCID 20437385—
ProductHCID 178418529HCID 178418529—

Reaction Steps

A solution of 3-methylbutylmagnesium bromide is prepared by treating 15.1 g. of 3-methylbutyl bromide with 2.7 g. of magnesium turnings in 50 ml. dry tetrahydrofuran. The resultant Grignard reagent is dropwise added to a cold (-10° C.) solution of 36.1 g. of 1,12-dibromododecane and 0.2 g. of Li2CUCl4 in 75 ml. dry tetrahydrofuran. The solution is stirred for 1 hour, evaporated, and fractionally distilled in vacuo to yield 15-methylhexadecyl bromide as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242273
Source datasetuspto-grants-1980_12
ORD IDord-96680e06c59d4db8963970b08b1287df
Source noteuspto-grants-1980_12