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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591993Generated: November 1, 2026

Azobisisobutyronitrile → HCID 67138806, compound

https://huagongshe.com/reaction/1591993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methyl-thiophene-2-carboxylic acid 2-trimethylsilanylethyl esterHCID 67138429—
CatalystMercuryHCID 23931—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 67138806HCID 67138806—

Reaction Steps

A solution of the title A compound, 5-methyl-thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester (34.15 g, 141 mmol) in CCl4 (200 mL) is treated with N-bromosuccinimide (NBS, 25.08 g, 141 mmol) and 2,2′-azobisisobutyronitrile (1.0 g, 6 mmol). The mixture is irradiated with a 450 W mercury lamp for 3 h. An additional 2.5 g of NBS is added and the mixture is further irradiated for 2 h. The mixture is filtered through Celite and a plug of silica gel. The solvent is evaporated to give 5-bromomethyl-thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291635B2
Source datasetuspto-grants-2007_11
ORD IDord-5a721372e7a4485aab64850f49bc6764
Source noteuspto-grants-2007_11