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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744409Generated: October 25, 2026

Azobisisobutyronitrile → 5-(Bromomethyl)thiophene-2-carbonitrile

https://huagongshe.com/reaction/1744409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methylthiophene-2-carbonitrileHCID 312733—
ReactantNbs aibnHCID 86630000—
Product5-(Bromomethyl)thiophene-2-carbonitrileHCID 10560016—

Reaction Steps

1.69 kg (9.51 moles) of NBS and 156 g (0.95 moles) of AIBN were well mixed and placed in a vinyl wrapper (at this time, the previous reaction was regarded to be proceeded to 100%). The benzene solution of Example 2 was heated. The NBS-AIBN mixture was portionwise added to the heated solution at 73° C. for 40 minutes. The solution was refluxed for 1.5 hours after the addition was done. After confirming completion of the reaction by HPLC, the solution was cooled to room temperature. The reaction solution was washed with [1 L of H2O+4 L of 5% NaHCO3], and then [2 L of H2O+1 L of 5% NaCl].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015337B2
Source datasetuspto-grants-2006_03
ORD IDord-2f748aa9f05543a6be1386a4cd7d79dc
Source noteuspto-grants-2006_03