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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505659Generated: November 3, 2026

Azobisisobutyronitrile → HCID 90404280, compound

https://huagongshe.com/reaction/1505659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 90404947HCID 90404947—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 90404280HCID 90404280119%

Reaction Steps

To a stirred solution of 561 mg of tert-butyl 2-cyano-4-methoxy-5-methyl-1H-indole-1-carboxylate (1.96 mmol) in carbon tetrachloride (9 mL) was added 349 mg of N-bromosuccinimide (1.96 mmol) and 64 mg of AIBN (0.39 mmol). The mixture was refluxed for 1 h, then cooled and concentrated and filtered through short silica gel plug using hexane-ethyl acetate 10:1 to give 852 mg of crude tert-butyl 5-(bromomethyl)-2-cyano-4-methoxy-1H-indole-1-carboxylate that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216993B2
Source datasetuspto-grants-2015_12
ORD IDord-061259343eb343d6840f12f313fa78e6
Source noteuspto-grants-2015_12