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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989817Generated: November 2, 2026

2-(3-Bromo-4-methoxyphenyl)-2-methylpropanal → 2-Bromo-4-(1,1-dimethyl-allyl)-1-methoxy-benzene

https://huagongshe.com/reaction/1989817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Bromo-4-methoxyphenyl)-2-methylpropanalHCID 11161190—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-4-(1,1-dimethyl-allyl)-1-methoxy-benzeneHCID 11242261—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of methyltriphenylphosphonium bromide (7.71 g, 0.0215 mol) in dry THF (100 mL) was cooled to 0° C. under argon. n-BuLi (2.5M, 8 mL, 0.020 mol) was added slowly. The resulting clear orange solution of the ylide was stirred for another 15 min at 0° C. 2-(3-Bromo-4-methoxy-phenyl)-2-methyl-propionaldehyde (3.7 g, 0.014 mol) was dissolved in dry THF (50 mL) and added to ylide-solution. The mixture was stirred for 3 h/25° C. and the resulting suspension was quenched with MeOH (10 mL). The solvent was removed under reduced pressure and the crude product was purified by flash chromatography using n-heptane as eluent. Yield: 3.1 g (84%). GCMS: >99%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642367B2
Source datasetuspto-grants-2010_01
ORD IDord-8aa25e99d5f64f8f8502362ecd780eb6
Source noteuspto-grants-2010_01