Hydrochloric Acid → 4,4'-Dimethoxybibenzyl

HRID 1583558

Reaktionsgleichung

Reaktionsgleichung von HRID 1583558
[C:1]1([C:9]([CH2:11][C:12]2[CH:19]=[CH:18][C:15]([O:16][CH3:17])=[CH:14][CH:13]=2)=O)[CH:8]=[CH:7][C:4]([O:5][CH3:6])=[CH:3][CH:2]=1.O1CCOCC1.Cl>[Zn].C1(C)C=CC=CC=1>[CH3:17][O:16][C:15]1[CH:14]=[CH:13][C:12]([CH2:11][CH2:9][C:1]2[CH:2]=[CH:3][C:4]([O:5][CH3:6])=[CH:7][CH:8]=2)=[CH:19][CH:18]=1

Komponenten

6

Edukt 3

HCID 313Hydrochloric Acid2×HCID 312751,4-DioxaneHCID 67120Desoxyanisoin

Produkt 1

HCID 742614,4'-Dimethoxybibenzyl

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 1140TolueneLösungsmittel

Versuchsvorschrift

A mixture of 60 g of desoxyanisoin, 120 g of amalgamated zinc, 200 ml of dioxane, 100 ml of toluene and 200 ml of concentrated hydrochloric acid was refluxed for 24 hours. Another 50 ml of concentrated hydrochloric acid was added after the first 6 hours. The reaction mixture was cooled to room temperature and the organic layer was separated and mixed with 300 ml of ethyl acetate. It was washed with water, dried over anhydrous magensium sulfate and concentrated to give 26 g of white waxy solid.

Aufarbeitung

  1. temperaturewas refluxed for 24 hours
  2. customthe organic layer was separated
  3. additionmixed with 300 ml of ethyl acetate
  4. washIt was washed with water
  5. dry with materialdried over anhydrous magensium sulfate
  6. concentrationconcentrated
  7. customto give 26 g of white waxy solid

Quellen und Nachweise

ORD-Eintrag
ord-6415fd7e238c4f79971896db86086bba
Quelldatensatz
uspto-grants-1985_11
Patentnummer
US04552876

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