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1,5-Pentanediol → 5-(2-Nonyloxy)pentanol

HRID 36136
ノート
印刷プレビュー

反応式

HRID 36136 の反応式
[CH2:1]([OH:7])[CH2:2][CH2:3][CH2:4][CH2:5][OH:6].[CH2:8]=[CH:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[OH-].[Na+].[BH4-].[Na+]>CN(C)C=O>[CH3:8][CH:9]([O:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:7])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 81051,5-PentanediolHCID 14798Sodium HydroxideHCID 312851-NoneneHCID 4311764Sodium borohydride

生成物 1

HCID 536516505-(2-Nonyloxy)pentanol

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a mixture of 12.6 grams of mercuric acetate and 8.3 grams of 1,5-pentanediol in 100 ml of dimethylformamide is added 5.0 grams of 1-nonene. The mixture is stirred at room temperature for ten minutes and 40 ml of an aqueous NaOH solution (3 Molar) is added followed by 40 ml of an aqueous NaBH4 solution (0.5 Molar in 3 Molar NaOH). The solution is decanted from the mercuric salts and concentrated. The residue is partitioned between ethyl acetate and water and the organic layer is washed with brine, dried over sodium sulfate, filtered, and concentrated under vacuum to give a clear liquid. This liquid is flash chromatographed, initially with a 19 to 1 ratio of hexane to ethyl acetate and, subsequently, with a 9 to 1 ratio, to give 5-(2-nonyloxy)pentanol as a clear liquid.

後処理

  1. customThe solution is decanted from the mercuric salts
  2. concentrationconcentrated
  3. customThe residue is partitioned between ethyl acetate and water
  4. washthe organic layer is washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under vacuum
  8. customto give a clear liquid
  9. customchromatographed, initially with a 19 to 1 ratio of hexane to ethyl acetate

出典と根拠

ORDレコード
ord-00aeb6324f474d8e98751a06f7e11cdd
出典データセット
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05412137

反応ノート

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