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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654112Generated: November 1, 2026

N-bromobutanimide → 2-(Bromomethyl)-4-(trifluoromethyl)furan

https://huagongshe.com/reaction/1654112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methyl-4-(trifluoromethyl)furanHCID 21819750—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-4-(trifluoromethyl)furanHCID 2181975360.1%

Reaction Steps

6 g of the product of Stage D were refluxed for 1 and a half hours in 50 ml of carbon tetrachloride in the presence of 7.2 g of N-bromosuccinimide and 0.3 g of azobisisobutyronitrile and the mixture was allowed to return to room temperature and was filtered. The solvent was evaporated and the residue was chromatographed on silica (eluent: 98/2 ether/isopropyl ether) to obtain 5.5 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405865
Source datasetuspto-grants-1995_04
ORD IDord-b3d89a00b8414e9d93c3bacac0ffbde1
Source noteuspto-grants-1995_04