HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → {[1-(2,4-Dichlorophenyl)vinyl]sulfonyl}benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-(2,4-Dichlorophenyl)-2-(phenylsulfonyl)ethyl acetate | HCID 58914794 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {[1-(2,4-Dichlorophenyl)vinyl]sulfonyl}benzene | HCID 58914799 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250443B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-6c7cc023e0d64bf1b451a38306f0d605 |
| Source note | uspto-grants-2007_07 |