Hydrochloric Acid → 2-Chloro-1,1-bis(4-chlorophenyl)ethan-1-ol

HRID 1723067Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1723067
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][CH:3]=1.[Mg].[Cl:10][CH2:11][C:12]([O:14]CC)=O.[ClH:17]>CCOCC>[Br-:1].[Cl:8][C:5]1[CH:6]=[CH:7][C:2]([C:12]([C:2]2[CH:7]=[CH:6][C:5]([Cl:17])=[CH:4][CH:3]=2)([OH:14])[CH2:11][Cl:10])=[CH:3][CH:4]=1

Komponenten

7

Versuchsvorschrift

Part A. A solution of 4-chlorobenzenemagnesium bromide was prepared in ether (800 mL) from 4-bromochlorobenzene (114.9 g, 0.6 mole) and magnesium chips (15.1 g, 0.62 mole). This mixture was cooled to 0°, and a solution of ethyl chloroacetate (24.5 g, 0.2 mole) was added dropwise. When addition was complete, stirring was continued at 0° for an additional hour. 1 N hydrochloric acid was then added, and the mixture extracted with dichloromethane. The organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was distilled in a kugelrohr apparatus at 0.1 torr and 180°-200° to provide 1,1-bis(4-chlorophenyl)-2-chloroethanol (43.1 g, 71%) as an oil. NMR(CDCl3) 7.33(8H,m) 4.11(2H,s) 3.17(1H,s). IR (neat film) 3551 cm-1.

Aufarbeitung

  1. temperatureThis mixture was cooled to 0°
  2. additionWhen addition
  3. waitwas continued at 0° for an additional hour
  4. extractionthe mixture extracted with dichloromethane
  5. washThe organic phase was washed with water
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated under reduced pressure
  8. distillationThe residue was distilled in a kugelrohr apparatus at 0.1 torr and 180°-200°

Quellen und Nachweise

ORD-Eintrag
ord-19d044bdb81a453cb69f9690a0dc420f
Quelldatensatz
uspto-grants-1989_08
Patentnummer
US04859693

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