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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654406Generated: November 3, 2026

Tributylstannane → HCID 19887190, compound

https://huagongshe.com/reaction/654406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 53802832HCID 53802832—
SolventBenzeneHCID 241—
ProductHCID 19887190HCID 19887190—

Reaction Steps

N-(2-Butenyl)-N-(3-trifluoromethylphenyl)-2-chloro-2-(3,5-difluorophenyl)acetamide (1.6 g) was added to 30 ml of benzene, followed by the addition of 1.1 ml of tributyltin hydride and a catalytic amount of α,α-azobisisobutyronitrile (AIBN) under stirring at the refluxing temperature. The reaction mixture was then stirred for 20 minutes at the refluxing temperature. The reaction mixture was then concentrated in an evaporator. The resultant concentrate was purified by chromatography on a silica gel, whereby 0.75 g of the 3,4-trans isomer of 4-ethyl-3-(3,5-difluorophenyl)-1-(3-trifluoromethylphenyl)-2-pyrrolidinone and 0.14 g of its 3,4-cis isomer were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05131947
Source datasetuspto-grants-1992_07
ORD IDord-386a28b0206b42b8adf262c3bd743bc4
Source noteuspto-grants-1992_07