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Bromide ion → 5-(Cyclopent-1-enyl)-2-methylpentan-2-ol

HRID 2187326
ノート
印刷プレビュー

反応式

HRID 2187326 の反応式
[C:1]1([CH2:6][CH2:7][CH2:8][C:9](=[O:11])[CH3:10])[CH2:5][CH2:4][CH2:3][CH:2]=1.[Br-].Cl.[CH2:14](OCC)C>>[C:1]1([CH2:6][CH2:7][CH2:8][C:9]([CH3:14])([OH:11])[CH3:10])[CH2:5][CH2:4][CH2:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 259Bromide ionHCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 135280095-(1-Cyclopentenyl)pentan-2-one

生成物 1

HCID 184338735-(Cyclopent-1-enyl)-2-methylpentan-2-ol収率 11%

実験手順

5-(Cyclopent-1-enyl)-2-pentanone (5.95 g; 39 mmol) in ethyl ether (6 ml) was added dropwise to a 3M solution of methylnagnesium bromide in the same solvent (17 ml; 51 mmol) during 15 minutes. After 2 hours at reflux, the mixture was cooled down to room temperature, poured into ice (20 g), acidified with 5N HCl (20 ml) and extracted with MTBE (60 ml). The aqueous phase was separated and extracted again with MTBE (2×100 ml). The combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml), dried over MgSO4 and concentrated in vacuo. Bulb-to-bulb distillation (80° C./0.06 torr) yielded quantitatively 5.84 g of 5-(cyclopent-1-enyl)-2-methylpentan-2-ol containing 11% of 5-cyclopentylidene-2-methylpentan-2-ol.

後処理

  1. temperatureAfter 2 hours at reflux
  2. extractionextracted with MTBE (60 ml)
  3. customThe aqueous phase was separated
  4. extractionextracted again with MTBE (2×100 ml)
  5. washThe combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. distillationdistillation (80° C./0.06 torr)

出典と根拠

ORDレコード
ord-13540fe1e8c841bc8238ffba1ff52f14
出典データセット
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06410000B1

反応ノート

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