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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823701Generated: October 30, 2026

Toluene → HCID 22146252, compound

https://huagongshe.com/reaction/1823701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAcetonitrileHCID 6342—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22146239HCID 22146239—
SolventWaterHCID 962—
ProductHCID 22146252HCID 22146252—

Reaction Conditions

Temperature0 °C

Reaction Steps

1,2-Bis(2-methylbutyloxy)benzene (338 g, 1.35 mol) together with 2.5 l of acetonitrile was placed in a reaction vessel, cooled to 0° C. and admixed with 264 g (1.48 mol) of N-bromosuccinimide. The mixture was warmed to RT and stirred for another 90 minutes. After taking off the acetonitrile, the residue was admixed with toluene and water and the phases were separated. After shaking the aqueous phase with toluene and drying the organic phase over Na2SO4, the toluene was taken off. The crude product was purified by double fractional distillation under reduced pressure. This gave the product as a colorless oil (145° C., 1.3 mbar): 275 g (62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041388B1
Source datasetuspto-grants-2006_05
ORD IDord-4e6c824e384947cba43c6849e5aab398
Source noteuspto-grants-2006_05