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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297502Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → {[1-(2,4-Dichlorophenyl)vinyl]sulfonyl}benzene

https://huagongshe.com/reaction/1297502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-(2,4-Dichlorophenyl)-2-(phenylsulfonyl)ethyl acetateHCID 58914794—
SolventTetrahydrofuranHCID 8028—
Product{[1-(2,4-Dichlorophenyl)vinyl]sulfonyl}benzeneHCID 5891479997%

Reaction Steps

DBU (1.5 eq) in THF was added to a solution of 2-(2,4-dichlorophenyl)-2-(phenylsulfonyl)ethyl acetate (3) (1 eq) in THF at rt. After stirring for 40 min., the reaction was quenched with sat. aq. NH4Cl. The layers were separated, and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated under reduced pressure to give the {[1-(2,4-dichlorophenyl)vinyl]sulfonyl}benzene (4) (97% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250443B2
Source datasetuspto-grants-2007_07
ORD IDord-6c7cc023e0d64bf1b451a38306f0d605
Source noteuspto-grants-2007_07