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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774306Generated: October 31, 2026

1-Bromo-2-methylpropane → HCID 25212074, compound

https://huagongshe.com/reaction/1774306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methylpropaneHCID 6555—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 58531816HCID 58531816—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetoneHCID 180—
ProductHCID 25212074HCID 25212074—

Reaction Steps

With reference to Scheme 1, compound 4 (0.5 g, 1.3 mmol) and K2CO3 (0.5 g) was suspended in acetone (10 ml) followed by addition of TBAI (50 mg). To this mixture, isobutyl bromide (0.3 ml, 2.8 mmol) was added slowly. The reaction was refluxed for 3 h and quenched with water (50 ml). The aqueous phase was extracted with ethyl acetate (20 ml) twice. The combined organics was washed with brine and dried over sodium sulfate. Removal of the solvent gave a yellow oil residue, which was purified by chromatography on silica gel (elute with CH2Cl2/EtOAc 1:1) to give a mixture of compound 5 and 6 as light yellow oil (0.45 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260391B2
Source datasetuspto-grants-2016_02
ORD IDord-b39289a7c0ec44fb970c39b73473cb0c
Source noteuspto-grants-2016_02