Water → cis-1,2-Cyclooctanediol

HRID 1392735ノート

反応式

HRID 1392735 の反応式
[CH:1]1CC[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.C[N+]1([O-])[CH2:15][CH2:14][O:13]CC1.[OH2:17]>C(#N)C.[Os](=O)(=O)(=O)=O>[C@@H:14]1([OH:13])[CH2:15][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C@@H:1]1[OH:17]

参加物

6

反応物 3

HCID 962WaterHCID 136091-CycloocteneHCID 82029Methyl morpholine oxide

生成物 1

HCID 10888034cis-1,2-Cyclooctanediol

試薬・触媒・溶媒 2

HCID 30318Osmium Tetroxide触媒HCID 6342Acetonitrile溶媒

反応条件

温度
45 °C

実験手順

Cyclooctene (4.41 g) was dissolved in acetonitrile (45 ml) and water (15 ml), and to the solution N-methylmorpholine N-oxide (5.15 g) and microcapsulated osmium tetroxide (1 g, containing 10% osmium tetroxide) were added, and the mixture was stirred at 40 to 50° C. for 21 hours. Insoluble microcapsulated osmium tetroxide was removed by filtration, and washed with acetonitrile, and the filtrate was concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel (hexane:ethyl acetate=1:1) to obtain the title compound (4.97 g).

後処理

  1. customInsoluble microcapsulated osmium tetroxide was removed by filtration
  2. washwashed with acetonitrile
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe residue was purified by flash column chromatography on silica gel (hexane:ethyl acetate=1:1)

出典と根拠

ORDレコード
ord-992deafe31bf4d49a3836e6cd2cd1d77
出典データセット
uspto-grants-2008_03
特許番号
US07342014B2

反応ノート

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