Acetonitrile → 1-Cyano-2-(cyanomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalene

HRID 6397

反応式

HRID 6397 の反応式
C(NC(C)C)(C)C.C([Li])CCC.[C:13](#[N:15])[CH3:14].[C:16]([C:18]1[C:27]2[C:22](=[CH:23][C:24]([O:28][CH3:29])=[CH:25][CH:26]=2)[CH2:21][CH2:20][CH:19]=1)#[N:17]>C1COCC1>[C:13]([CH:14]1[C:27]2[C:22](=[CH:23][C:24]([O:28][CH3:29])=[CH:25][CH:26]=2)[CH2:21][CH2:20][CH:19]1[CH2:18][C:16]#[N:17])#[N:15]

参加物

6

反応物 4

HCID 6342AcetonitrileHCID 7912DiisopropylamineHCID 30144661-Naphthalenecarbonitrile, 3,4-dihydro-6-methoxy-2 回HCID 178418339Butyllithium

生成物 1

HCID 197932931-Cyano-2-(cyanomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalene収率 74.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒4 回

反応条件

温度
-78 °C

実験手順

To a solution of 1.05 mL (7.5 mmol) of diisopropylamine in 10 mL of THF at -78° C., under a nitrogen atmosphere, was added n-butyllithium (2.2 mL of a 2.5M solution in THF, 5.5 mmol) and the resultant solution was stirred at -78° C. for 40 min. To the stirred solution was added, dropwise over a 25 minute period, a solution of 274 μL (5.25 mmol) of acetonitrile in 5 mL of THF. The solution was stirred for 20 min at -78° C. and then a solution of 926 mg (5 mmol) of 1-cyano-6-methoxy-3,4-dihydronaphthalene (the product of Step 2 of Example 1) in 5 mL of THF was added via syringe pump over a 20 min period. The reaction mixture then allowed to warm to ambient temperature and was stirred at ambient temperature for 1 h and then the reaction was quenched by pouring the reaction mixture into and then the reaction was quenched by pouring the reaction mixture into saturated aqueous ammonium chloride solution. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography on silica gel eluted with 25% ethyl acetate in hexane to give 840 mg (74% yield) of the title compound as a 1:1 mixture of the cis and trans isomers; MS DCl--NH3M/Z: 244 (M+H)+.

後処理

  1. additionTo the stirred solution was added, dropwise over a 25 minute period
  2. stirringThe solution was stirred for 20 min at -78° C.
  3. temperatureto warm to ambient temperature
  4. stirringwas stirred at ambient temperature for 1 h
  5. customthe reaction was quenched
  6. additionby pouring the reaction mixture into and then the reaction
  7. customwas quenched
  8. additionby pouring the reaction mixture into saturated aqueous ammonium chloride solution
  9. customThe layers were separated
  10. extractionthe aqueous layer was extracted with ethyl acetate
  11. dry with materialThe combined organic layers were dried over anhydrous magnesium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated in vacuo
  14. customThe residue was purified by chromatography on silica gel
  15. washeluted with 25% ethyl acetate in hexane

出典と根拠

ORDレコード
ord-2381c22df2194b6c83a6f440b9b07972
出典データセット
uspto-grants-1993_09
特許番号
US05248677

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