tert-Butanol → HCID 67108500, Verbindung

HRID 471882

Reaktionsgleichung

Reaktionsgleichung von HRID 471882
[CH2:1]([O:3][C:4]([C:6]1(CC=C)[CH2:11][CH2:10][CH2:9][CH:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:7]1)=[O:5])[CH3:2].C(=O)([O-])[O-:21].[K+].[K+].N12CCC(CC1)CC2.S([O-])([O-])=O.[Na+].[Na+].[C:40]([OH:44])(C)([CH3:42])[CH3:41]>O.[Fe-3](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+]>[CH2:1]([O:3][C:4]([C:6]1([CH2:41][CH:40]([OH:44])[CH2:42][OH:21])[CH2:11][CH2:10][CH2:9][CH:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:7]1)=[O:5])[CH3:2]

Komponenten

8

Versuchsvorschrift

To a solution of 1-allyl-cyclohexane-1,3-dicarboxylic acid diethyl ester from step 2 (250 g, 0.93 mol) in t-butanol (2.3 L) and water (2.3 L) was added potassium ferricyanide (920 g, 2.79 mol), potassium carbonate (386 g, 2.79 mol), potassium osmate dihydrate (4.75 g, 13 mmol) and quinuclidine (0.073 g, 7.0 mmol). The resulting dark colored solution was stirred at rt overnight and then quenched with portion-wise addition of sodium sulfite (1.05 kg, 8.37 mol). After dilution with ethyl acetate, it was extracted, washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure. The resulting residue (224 g) was used in the next step without delay and without further purification.

Aufarbeitung

  1. extractionAfter dilution with ethyl acetate, it was extracted
  2. washwashed with water and brine
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated under reduced pressure
  5. customThe resulting residue (224 g) was used in the next step without delay and without further purification

Quellen und Nachweise

ORD-Eintrag
ord-7468b90972ee44d690b9f8ca57c7a586
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08633190B2

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