Iodine → 1-(4'-Hydroxy-n-hexyl)-1-cyclohexanol

HRID 420883

反応式

HRID 420883 の反応式
BrCCCCCBr.[Mg].II.Br[C:12](Br)([CH2:15][CH3:16])[CH2:13][CH3:14].[CH:18]1([CH2:25][C:26](=[O:28])[CH3:27])[CH2:24][CH2:23][CH2:22]CCC1.C1C[O:32]CC1>>[OH:32][CH:12]([CH2:15][CH3:16])[CH2:13][CH2:14][CH2:27][C:26]1([OH:28])[CH2:22][CH2:23][CH2:24][CH2:18][CH2:25]1

参加物

7

実験手順

A solution of 1,5-dibromopentane (5.66 gms, 24.6 mmol) in dry THF (30 ml) was added slowly to a suspension of Magnesium turning (3.2 gms, 131 mmole) in dry THF (70 ml) and catalytic amount of iodine under nitrogen atmosphere. After the addition of about 5 ml of dibromopentane solution in THF, Grignard reaction was initiated. The addition was continued maintaining a gentle reflux. The mixture was refluxed for 18 hours to complete the formation of the Grignard reagent. To the reaction mixture was added a solution of a solution of lactone (20, 3 gms, 23.4 mmol) in dry THF (20 ml). The resulting mixture was refluxed for 10 hours under nitrogen and then quenched by addition of saturated solution of ammonium chloride at 0° C. The product was extracted in ethylacetate. Organic layer was washed with water, brine and dried over anh. Na2SO4. Drying agent was filtered off and the solvent was removed under vacuum to give 2.8 gms of diol (21), which was used without any further purification in the next step.

後処理

  1. additionThe addition
  2. temperaturewas continued maintaining a gentle reflux
  3. temperatureThe mixture was refluxed for 18 hours
  4. temperatureThe resulting mixture was refluxed for 10 hours under nitrogen
  5. customquenched by addition of saturated solution of ammonium chloride at 0° C
  6. extractionThe product was extracted in ethylacetate
  7. washOrganic layer was washed with water, brine
  8. dry with materialdried over anh. Na2SO4
  9. customDrying agent
  10. filtrationwas filtered off
  11. customthe solvent was removed under vacuum

出典と根拠

ORDレコード
ord-4d9c20739238480c818c82204f75668c
出典データセット
uspto-grants-2012_01
特許番号
US08097728B2

関連ノート

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