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Methanol → 3-Ethynyl-1-azabicyclo[2.2.2]octan-3-ol

HRID 580985
ノート
印刷プレビュー

反応式

HRID 580985 の反応式
[C:1]([C:3]1([O:11]C(=O)CCC)[CH:8]2[CH2:9][CH2:10][N:5]([CH2:6][CH2:7]2)[CH2:4]1)#[CH:2].CO.[OH-].[Na+].S([O-])([O-])(=O)=O.[NH4+].[NH4+]>O>[C:1]([C:3]1([OH:11])[CH:8]2[CH2:9][CH2:10][N:5]([CH2:6][CH2:7]2)[CH2:4]1)#[CH:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 887MethanolHCID 14798Sodium Hydroxide2 回HCID 6097028Ammonium SulfateHCID 54501015HCID 54501015、化合物

生成物 1

HCID 36135173-Ethynyl-1-azabicyclo[2.2.2]octan-3-ol収率 18.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

A solution of (±)-3-ethynyl-3-butyryloxyquinuclidine (4.42 g) in deionised water (700 ml) containing methanol (35 ml) was adjusted to pH 7.0 using an 0.1M aqueous sodium hydroxide solution (dispensed by a pH autotitrater). A suspension of pig liver esterase (8.0 ml, 9200 units,in 3.2M aqueous ammonium sulphate solution at pH 8; S1 gma Chemical Company Ltd) was added to the reaction mixture and the mixture was stirred at ambient temperature whilst maintaining the pH at 7.0 using 0.1M aqueous sodium hydroxide solution (dispensed by a pH autotitrater). After 5.5 hours, 7.3 ml of the sodium hydroxide solution had been consumed, indicating that the hydrolysis was 35% complete. The pH of the reaction mixture was adjusted to 2.5 using 2H aqueous hydrochloric acid and the mixture was stirred for 10 minutes. 2M aqueous sodium hydroxide solution was then added to the mixture to give a pH of 7.05 and the mixture extracted with diethyl ether (3×200 ml, followed by 12×150 ml). The aqueous phase was separated, and freeze dried over a period of 48 hours to give a solid which was dissolved in deionised water (30 ml). The solution was filtered and the filtrate was basified to pH 9 using 10.8M sodium hydroxide solution to give a solid. The solid was collected by filtration to give (+)-3-ethynyl-3-hydroxyquinuclidine, (554 mg), m.p. 204-207° C., [α]20D =+54.5° (C=0.99, methanol).

後処理

  1. additionwas added to the reaction mixture
  2. custom7.3 ml of the sodium hydroxide solution had been consumed
  3. stirringthe mixture was stirred for 10 minutes
  4. addition2M aqueous sodium hydroxide solution was then added to the mixture
  5. customto give a pH of 7.05
  6. extractionthe mixture extracted with diethyl ether (3×200 ml, followed by 12×150 ml)
  7. customThe aqueous phase was separated
  8. customfreeze dried over a period of 48 hours
  9. customto give a solid which
  10. filtrationThe solution was filtered
  11. customto give a solid
  12. filtrationThe solid was collected by filtration

出典と根拠

ORDレコード
ord-f84f0c9d5b9c428190c9213918765cb2
出典データセット
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05919793

反応ノート

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