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Cyclohexanol, 3,3-dimethyl- → HCID 58495453、化合物

HRID 1190971
ノート
印刷プレビュー

反応式

HRID 1190971 の反応式
[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][CH2:5][CH:4]([OH:8])[CH2:3]1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].Cl[C:21]1[CH:26]=[CH:25][C:24]([C:27]#[N:28])=[CH:23][N:22]=1>C1COCC1>[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][CH2:5][CH:4]([O:8][C:21]2[N:22]=[CH:23][C:24]([C:27]#[N:28])=[CH:25][CH:26]=2)[CH2:3]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 79105Cyclohexanol, 3,3-dimethyl-HCID 2724254Sodium bis(trimethylsilyl)amideHCID 51520946-Chloro-3-pyridinecarbonitrile

生成物 1

HCID 58495453HCID 58495453、化合物収率 84.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

Dissolve 3,3-dimethylcyclohexanol (6 g, 47 mmoles) in anhydrous THF (70 mL) under nitrogen atmosphere and cool at −78° C. Add sodium bis(trimethylsilyl)amide (23.4 mL, 47 mmol, 2M solution in THF) to this solution and stir at −78° C. for 30 min before raising to room temperature. Cool down again to −78° C. and add a solution of 2-chloro-5-cyanopyridine (7.1 g, 51.7 mmoles) in anhydrous THF (20 mL) and stir overnight while warming to room temperature. Add saturated aqueous NaHCO3 (100 mL) and extract the aqueous layer with DCM (3×100 mL). Wash the combined organic extracts with brine (200 mL). Dry over MgSO4, filter and concentrate in vacuo. Purify the crude mixture by chromatography on silica gel eluting with cyclohexane/EtOAc (1:0 to 9:1 gradient) to afford the desired intermediate as a solid (9.14 g, 84%). MS (ES+) m/z: 231.1 (M+H)+.

後処理

  1. temperaturebefore raising to room temperature
  2. temperatureCool down again to −78° C.
  3. temperaturewhile warming to room temperature
  4. extractionAdd saturated aqueous NaHCO3 (100 mL) and extract the aqueous layer with DCM (3×100 mL)
  5. washWash the combined organic extracts with brine (200 mL)
  6. dry with materialDry over MgSO4
  7. filtrationfilter
  8. concentrationconcentrate in vacuo
  9. customPurify the crude mixture by chromatography on silica gel eluting with cyclohexane/EtOAc (1:0 to 9:1 gradient)

出典と根拠

ORDレコード
ord-7e8d7a57d9454887acc99e819d781b9c
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08680091B2

反応ノート

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