Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439935Generated: October 27, 2026

1-Bromo-3-methylbutane → 1-Bromo-4-isopentylthiobenzene

https://huagongshe.com/reaction/439935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methylbutaneHCID 7891—
ReactantSodium HydroxideHCID 14798—
Reactant4-BromothiophenolHCID 66049—
SolventAcetoneHCID 180—
Product1-Bromo-4-isopentylthiobenzeneHCID 12521243—

Reaction Steps

A mixture of 15 g (79 mmol) of 4-bromo-thiophenol (Compound 40), 3.16 g (79 mmol) of powdered sodium hydroxide and 150 ml of acetone was heated at reflux for 15 minutes. The refluxing mixture was then treated dropwise with a solution of 12 g (79 mmol) of 1-bromo-3-methylbutane (Compound 49) in 25 ml of acetone and then refluxed for a further 18 hours. The mixture was allowed to cool and the solvent removed in-vacuo. The residue was taken up in 25 ml of water and the mixture basified with 2N NaOH solution. The mixture was extracted with ether and the combined ether extracts washed successively with 1N NaOH, water and saturated NaCl and then dried (MgSO4). The solvent was removed in-vacuo and the residue distilled (113-117 degrees C., 0.2 mm) to give the title compound as a colourless oil. PMR (CDCl3): & 0.93 (6H, d, J-6.6 Hz), 1.47-1.58 (2H, m), 1.65-1.80 (1H, m), 2.90 (2H, t, J-7.8 Hz), 7.18 (2H, d, J-8.6 Hz), 7.39 (2H, d, J-8.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516904
Source datasetuspto-grants-1996_05
ORD IDord-2f2b86566fd1493a8d217305a7f72176
Source noteuspto-grants-1996_05