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Dimethyl Sulfide → 1-[(E)-3-Chloro-1-methyl-1-propenyl]-3-nitrobenzene

HRID 1826401
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1826401
[Cl:1]N1C(=O)CCC1=O.CSC.[N+:12]([C:15]1[CH:16]=[C:17](/[C:21](/[CH3:25])=[CH:22]/[CH2:23]O)[CH:18]=[CH:19][CH:20]=1)([O-:14])=[O:13]>ClCCl>[Cl:1][CH2:23]/[CH:22]=[C:21](/[C:17]1[CH:18]=[CH:19][CH:20]=[C:15]([N+:12]([O-:14])=[O:13])[CH:16]=1)\[CH3:25]
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Komponenten

5

Edukt 3

HCID 1068Dimethyl SulfideHCID 31398ChlorosuccinimideHCID 69554909(E)-3-(3-nitrophenyl)-2-buten-1-ol

Produkt 1

HCID 695554961-[(E)-3-Chloro-1-methyl-1-propenyl]-3-nitrobenzene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a solution of N-chlorosuccinimide (52.3 g, 0.39 mol) in dichloromethane (800 ml) at 0° C. was added dropwise over 1 h dimethylsulfide (27.9 ml, 0.38 mol). To the mixture was added dropwise over 30 min at 0° C. a solution of (E)-3-(3-nitrophenyl)-2-buten-1-ol (Preparation 2, 72 g, 0.373 mol) in dichloromethane (200 ml). The mixture was warmed to room temperature over 1 h, then poured onto brine (500 ml). The layers were separated, and the aqueous layer extracted with ether (500 ml). The organic extracts were combined, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica column chromatography, eluting with 10:1 hexane/ethyl acetate, then as a gradient up to 4:1 hexane/ethyl acetate. Appropriate fractions were combined and concentrated in vacuo to give the title compound as a very pale yellow solid (69 g, 88%).

Aufarbeitung

  1. additionpoured onto brine (500 ml)
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted with ether (500 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by silica column chromatography
  8. washeluting with 10:1 hexane/ethyl acetate
  9. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-bfe0784f90034766b736d39f4b61c8e3
Quelldatensatz
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07049444B2

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