Water → Cyclopentadecanol

HRID 1883287

反応式

HRID 1883287 の反応式
[C:1]1(=[O:16])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CCCCCC.O>C(O)C>[CH:1]1([OH:16])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

参加物

5

実験手順

5.0 g of cyclopentadecanone (MW 224, 22.3 mmol) were dissolved in 5.0 ml of ethanol, and hydrogenated sodium borate (MW 37.8, 2.5 g) was added thereto over 30 minutes. During this period, the temperature of the reaction mixture increased from 20° C. to 50° C. After reaction for one hour at 50° C., 50 ml of hexane and 50 ml of water were successively added, and the reaction was terminated. The reaction mixture was separated into an aqueous phase and an organic phase. The organic phase was washed twice with water and the solvent was removed under reduced pressure to yield a crude product. 4.57 g of crude product were purified on a silica gel column chromatograph (internal diameter 25 mm×height 190 mm, silica gel 60 manufactured by Nakalai Tesque Co. Ltd.) using hexane:ethyl acetate (9:1, v/v), to give 2.35 g of cyclopentadecanol having a purity of 99.3%.

後処理

  1. waitDuring this period
  2. temperaturethe temperature of the reaction mixture increased from 20° C. to 50° C
  3. customAfter reaction for one hour at 50° C.
  4. customthe reaction was terminated
  5. customThe reaction mixture was separated into an aqueous phase
  6. washThe organic phase was washed twice with water
  7. customthe solvent was removed under reduced pressure
  8. customto yield a crude product
  9. custom4.57 g of crude product were purified on a silica gel column chromatograph (internal diameter 25 mm×height 190 mm, silica gel 60 manufactured by Nakalai Tesque Co. Ltd.)

出典と根拠

ORDレコード
ord-63a47636517a42099a5c4c752af81803
出典データセット
uspto-grants-2004_07
特許番号
US06759557B2

関連ノート

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