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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582459Generated: October 31, 2026

Azobisisobutyronitrile → HCID 54007580, compound

https://huagongshe.com/reaction/582459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 54094632HCID 54094632—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 54007580HCID 54007580—

Reaction Steps

A solution of 46 g (0.152 mol) of N-tert-butyl-2-methanesulfonyl-5-methyl-benzenesulfonamide in 450 ml of CCl4 is, after the addition of 27.0 g (0.152 mol) of NBS (N-bromosuccinimide) and 1 g of AIBN (azobisisobutyronitrile), heated under reflux for 7 h using a daylight lamp. The reaction mixture is then filtered and washed successively with NaHSO3 solution, NaHCO3 solution and water, dried over MgSO4 and completely concentrated in vacuo. 51.2 g of a crude mixture containing 55% by weight of N-tert-butyl-5-bromomethyl-2-methanesulfonylbenzenesulfonamide are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925596
Source datasetuspto-grants-1999_07
ORD IDord-c739353e925a491c99ae81b27c5f737b
Source noteuspto-grants-1999_07