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6-Oxoheptanal → 7-Hydroxyheptan-2-one

HRID 1527823
ノート
印刷プレビュー

反応式

HRID 1527823 の反応式
[O:1]=[C:2]([CH3:9])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]=[O:8]>C1(C)C=CC=CC=1>[OH:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][C:2](=[O:1])[CH3:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 110079176-Oxoheptanal

生成物 1

HCID 113670027-Hydroxyheptan-2-one

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

6-oxoheptanal (12.8 g, 0.1 mol.), toluene (76.8 g, 600 wt. %) and (ethylenediamine)[1,2-bis(diphenylphosphino)ethane]ruthenium (bispivalate) (9.6 mg, 0.0125 mmol, 0.0125 mol.%) were loaded altogether in a 200 ml autoclave equipped with a mechanical stirring device. Sealed autoclave was then purged under stirring with nitrogen (3 times to 5 bars) and hydrogen (3 times 5 bars) before being pressurized to 20 bars hydrogen. It was then heated to 90° C. and hydrogen pressure was maintained to 50 bars during all the reaction to afford desired product with 94% selectivity. Upon reaction completion (checked by both hydrogen consumption and GC), autoclave was then cooled down to 25° C. It was then depressurized and purged with nitrogen (3 times 5 bars) and reaction mixture was then transferred to a round-bottomed flask and solvent was removed under vacuum. After flash chromatography, 7-hydroxyheptan-2-one was obtained in 90% yield.

後処理

  1. customequipped with a mechanical stirring device
  2. customSealed autoclave
  3. customwas then purged
  4. temperaturehydrogen pressure was maintained to 50 bars during all
  5. customthe reaction

出典と根拠

ORDレコード
ord-c7f14b11a5f64910a783dca6baeece78
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09090534B2

反応ノート

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