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Sulfuric Acid → 2-((1S,2R,5S)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl)acetic acid

HRID 1912522
ノート
印刷プレビュー

反応式

HRID 1912522 の反応式
S(=O)(=O)(O)O.[CH3:6][C:7]1([CH3:17])[C@H:12]2[CH2:13][C@@H:8]1[CH2:9][CH2:10][C@@H:11]2CC#N.[CH2:18]([OH:20])[CH3:19].[OH:21]S(O)(=O)=O>C(O)C.O>[CH3:6][C:7]1([CH3:17])[C@H:12]2[CH2:13][C@@H:8]1[CH2:9][CH2:10][C@@H:11]2[CH2:19][C:18]([OH:21])=[O:20]
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

6

反応物 3

HCID 1118Sulfuric AcidHCID 687518342-((1S,2R,5S)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl)acetonitrileHCID 73950302Sulphuric acid ethanol

生成物 1

HCID 687539142-((1S,2R,5S)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl)acetic acid

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒2 回HCID 962
Water
溶媒

反応条件

温度
40 °C

実験手順

Concentrated sulfuric acid (33 mL) was added drop wise to ethanol (120 mL) at 0° C. A solution of Example 21B (7.20 g, 44.1 mmol) in ethanol (20 mL) was added to the ethanol-H2SO4 mixture. The mixture was heated at reflux for 24 hours. TLC showed a 1/1 mixture of ethyl ester and acid. The mixture was diluted with water. Ethanol was evaporated under reduced pressure and the mixture was extracted with ether. The organic extracts were dried with magnesium sulfate, filtered, and concentrated. The residue was dissolved in tetrahydrofuran (50 mL). To the mixture was added a solution of 25% NaOH (10 mL). The reaction was heated at 40° C. for 12 hours. The mixture was cooled at room temperature, tetrahydrofuran was evaporated, the mixture was diluted with brine and washed with ether (2×25 mL). The aqueous phase was acidified to pH 2 with 5 N HCl and extracted with ether (3×75 mL). The organic extracts were dried over magnesium sulfate, filtered, and concentrated to give the title compound.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 24 hours
  3. customEthanol was evaporated under reduced pressure
  4. extractionthe mixture was extracted with ether
  5. dry with materialThe organic extracts were dried with magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. dissolutionThe residue was dissolved in tetrahydrofuran (50 mL)
  9. additionTo the mixture was added a solution of 25% NaOH (10 mL)
  10. temperatureThe mixture was cooled at room temperature
  11. customtetrahydrofuran was evaporated
  12. additionthe mixture was diluted with brine
  13. washwashed with ether (2×25 mL)
  14. extractionextracted with ether (3×75 mL)
  15. dry with materialThe organic extracts were dried over magnesium sulfate
  16. filtrationfiltered
  17. concentrationconcentrated

出典と根拠

ORDレコード
ord-0c6d430143534843a6159d485e642904
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08609674B2

反応ノート

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