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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855269Generated: October 28, 2026

Diiodomethane → 1-Bromo-4-(1-methylcyclopropyl)benzene

https://huagongshe.com/reaction/855269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Bromo-4-(prop-1-en-2-yl)benzeneHCID 3614410—
ReactantHCID 178418750HCID 178418750—
SolventDichloromethaneHCID 6344—
SolventPentaneHCID 8003—
Product1-Bromo-4-(1-methylcyclopropyl)benzeneHCID 57374250570.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diethyl zinc (20.30 ml, 1M solution in hexane, 20.30 mmol) in DCM (25 ml) at 0° C. was added a solution of trifluoroacetic acid (1.56 ml, 20.30 mmol) in DCM (10 ml) dropwise. The mixture was stirred at 0° C. for 20 min and then a solution of CH2I2 (1.64 ml, 20.30 mmol) in DCM (10 ml) was added. After stirring for an additional 20 min a solution of 1-bromo-4-isopropenylbenzene (346 mg, 1.76 mmol) in DCM (10 ml) was added. The reaction mixture was slowly warmed to rt and stirring was continued for 16 h. Pentane was added and the mixture was washed with 1M HCl, sat. NaHCO3, sat. Na2SO3 and brine. The organic layer was dried (MgSO4), filtered, concentrated in vacuo to give a residue which was purified by flash column chromatography (100% pentane). The product (2.12 g, 86%) was isolated as a 4:1 mixture of product to methyleneiodide as a colorless oil. 1H NMR (CDCl3, 300 MHz): δ 7.38 (d, J=8.5 Hz, 2H), 7.12 (d, J=8.5 Hz, 2H), 1.37 (s, 3H), 0.84-0.79 (m, 2H), 0.76-0.71 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-6dfdceb85a044221b7f0eb2f0c9a37f1
Source noteuspto-grants-2007_08