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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464951Generated: October 29, 2026

Azobisisobutyronitrile → HCID 13210726, compound

https://huagongshe.com/reaction/464951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 20261491HCID 20261491—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 13210726HCID 13210726—

Reaction Steps

2.79 gm (0.01-ol) of 4-(p-chloro-phenyl)-2,6-dimethyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine were dissolved in 50 ml of carbon tetrachloride, the solution was heated at its boiling point with 1.8 gm of N-bromo-succinimide and 0.1 gm of azo-bis-isobutyronitrile for several hours. The resulting succinimide was suction-filtered off, and the solvent was removed in a rotary evaporator. The residue was admixed with a solution of 0.01 mol of sodium methoxide in methanol, and the mixture was heated at its boiling point for a short time. Then, water was added, and the resulting mixture was extracted with ether. Upon addition of etheral hydrochloric acid to the extract, the hydrochloride of the title compound crystallized out.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04550106
Source datasetuspto-grants-1985_10
ORD IDord-c9a5d1c0d9744681bfcf0d84847417a2
Source noteuspto-grants-1985_10