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Vinyl Acetate → (R)-methyl 9-hydroxy-10-undecenate

HRID 395932
ノート
印刷プレビュー

反応式

HRID 395932 の反応式
[OH:1][CH:2]([CH:14]=[CH2:15])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11].C(OC=C)(=O)C>C(OC(C)C)(C)C>[OH:1][C@@H:2]([CH:14]=[CH2:15])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11]
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

4

反応物 2

HCID 7904Vinyl AcetateHCID 11127632Methyl 9-hydroxy-10-undecenate

生成物 1

HCID 11736036(R)-methyl 9-hydroxy-10-undecenate収率 30.4%

試薬・触媒・溶媒 1

HCID 7914Diisopropyl Ether溶媒

反応条件

温度
30 °C

実験手順

To a solution of methyl 9-hydroxy-10-undecenate (500 mg) in diisopropyl ether (12 ml) was added vinyl acetate (323 μl) and Lipase PS (AMANO SEIYAKU Co., Ltd.) (500 mg) and then shaken for 62 hours at 30° C. The reaction mixture was filtrated and the filtrate was poured into ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate anhydride, and then evaporated under reduced pressure. The resulting product was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) to give (R)-methyl 9-hydroxy-10-undecenate (152 mg, 30.4%).

後処理

  1. filtrationThe reaction mixture was filtrated
  2. additionthe filtrate was poured into ethyl acetate
  3. washThe organic layer was washed with saturated brine
  4. dry with materialdried over magnesium sulfate anhydride
  5. customevaporated under reduced pressure
  6. customThe resulting product was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1)

出典と根拠

ORDレコード
ord-b46dbf12afe94e36857135fb52f2566b
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06605741B2

反応ノート

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