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Iodine → 4,4-Dimethyl-1-iodo-trans-1-octen-3-ol

HRID 67011
ノート
印刷プレビュー

反応式

HRID 67011 の反応式
C(BC(C(C)C)C)(C(C)C)C.[CH3:12][C:13]([CH3:28])([CH2:24][CH2:25][CH2:26][CH3:27])[CH:14]([O:17]C1CCCCO1)[C:15]#[CH:16].C([N+]([O-])(CC)CC)C.[OH-].[Na+].[I:39]I.S([O-])([O-])(=O)=S.[Na+].[Na+]>COCCOCCOC.O.O1CCCC1>[CH3:12][C:13]([CH3:28])([CH2:24][CH2:25][CH2:26][CH3:27])[CH:14]([OH:17])/[CH:15]=[CH:16]/[I:39]
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 6

HCID 807IodineHCID 14798Sodium HydroxideHCID 24477Sodium ThiosulfateHCID 123168Ethanamine, N,N-diethyl-, N-oxideHCID 192733Bis(1,2-dimethylpropyl)boraneHCID 145163702-[(4,4-Dimethyloct-1-YN-3-YL)oxy]oxane

生成物 1

HCID 20465723
4,4-Dimethyl-1-iodo-trans-1-octen-3-ol

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒HCID 8150Diglyme溶媒

実験手順

To 233 ml. of a 0.43 M solution of disiamylborane in diglyme cooled to 0° C. under an inert atmosphere is added 23.8 g. (0.100 mole) 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 995). The mixture is allowed to come to room temperature and is stirred at ambient temperature for 3 hours. The solution is cooled to 0° C. and 22.5 g. (0.30 mole) of triethylamine oxide is added portionwise such that the temperature is maintained at 0°-5° C. The mixture is stirred at 0° C. for 1 hour and is then poured into 150 ml. of 1 N sodium hydroxide followed immediately by a solution of 25.4 g. (0.100 mole) of iodine in 60 ml. of tetrahydrofuran. The mixture is stirred at ambient temperatures for 0.5 hour and poured into 500 ml. of water. The mixture is decolorized by addition of sodium thiosulfate solution and is extracted into ether. The organic phase is washed with water and the solvent is removed in vacuo. The residue is stirred at room temperature for 20 hours with 900 ml. 3:1:1 tetrahydrofuran-acetic acid-water. The solution is evaporated in vacuo and the residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene.

後処理

  1. additionis added 23.8 g
  2. customto come to room temperature
  3. temperatureThe solution is cooled to 0° C.
  4. temperatureis maintained at 0°-5° C
  5. stirringThe mixture is stirred at 0° C. for 1 hour
  6. additionis then poured into 150 ml
  7. stirringThe mixture is stirred at ambient temperatures for 0.5 hour
  8. additionpoured into 500 ml
  9. extractionis extracted into ether
  10. washThe organic phase is washed with water
  11. customthe solvent is removed in vacuo
  12. stirringThe residue is stirred at room temperature for 20 hours with 900 ml
  13. customThe solution is evaporated in vacuo
  14. customthe residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene

出典と根拠

ORDレコード
ord-f7dfc7d7d93e494a8dea7d9377943e16
出典データセット
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04343949

反応ノート

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