tert-Butanol → HCID 67108500、化合物

HRID 471882

反応式

HRID 471882 の反応式
[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]

参加物

8

反応物 5

HCID 6386tert-ButanolHCID 7527QuinuclidineHCID 11430Potassium CarbonateHCID 24437Sodium SulfiteHCID 67108610HCID 67108610、化合物

生成物 1

HCID 67108500HCID 67108500、化合物

試薬・触媒・溶媒 2

HCID 178511488HCID 178511488、化合物触媒HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7468b90972ee44d690b9f8ca57c7a586
出典データセット
uspto-grants-2014_01
特許番号
US08633190B2

関連ノート

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