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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250140Generated: November 1, 2026

Azobisisobutyronitrile → HCID 53938046, compound

https://huagongshe.com/reaction/1250140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 838711HCID 838711—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 53938046HCID 53938046—

Reaction Steps

A mixture of 2.2 g of methyl 2-(2-methylphenoxy)-3-methoxyacrylate, 1.78 g of N-bromosuccinimide, and a catalytic amount of azobisisobutyronitrile was heated at reflux in carbon tetrachloride for 4 hours. The solid was filtered, and the solvent evaporated to give crude methyl 2-(2-bromomethylphenoxy)-3-methoxyacrylate. A mixture of this crude material, 2.0 g of N-benzyloxy propionamide, and 3.9 g of caesium carbonate was heated at reflux in acetonitrile for 20 hours. The solid was filtered, the solvent evaporated, and the residue purified by silica gel chromatography to give methyl 2-{2-[(1-benzyloxyiminopropyl)oxymethyl]phenoxy}-3-methoxyacrylate (isomer Z) (0.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337306B1
Source datasetuspto-grants-2002_01
ORD IDord-9bdc1cd7be07478e8b3c3c3d54146f29
Source noteuspto-grants-2002_01