Water → HCID 20148855、化合物

HRID 1632628ノート

反応式

HRID 1632628 の反応式
[OH-:1].[Na+].[CH2:3]([N:10]1[C:14](=O)[CH2:13][CH:12]([CH2:16][C:17]#N)[CH:11]1[C:19]1[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=1[Cl:26])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[OH2:27]>>[CH2:3]([N:10]1[CH2:14][CH2:13][CH:12]([CH2:16][C:17]([OH:27])=[O:1])[CH:11]1[C:19]1[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=1[Cl:26])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

参加物

4

反応物 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 20148837HCID 20148837、化合物

生成物 1

HCID 20148855HCID 20148855、化合物

実験手順

To 90 ml of water containing 10 g of sodium hydroxide was added 5.0 g of 1-benzyl-3-cyanomethyl-2-(2,6-dichlorophenyl)-pyrrolidin-5-one. The reaction was refluxed 5 hours, cooled, and filtered. Extraction of the aqueous phase with ether followed by addition of ice and acidification with concentrated hydrochloric acid gave a solid which was then triturated with ether to yield beige crystals. Vacuum drying (0.1 Torr) under refluxing toluene for 15 hours followed by recrystallization from ethanol provided upon drying 1.50 g of colorless crystals, m.p. 186°-188°.

後処理

  1. temperatureThe reaction was refluxed 5 hours
  2. temperaturecooled
  3. filtrationfiltered
  4. extractionExtraction of the aqueous phase with ether
  5. additionfollowed by addition of ice and acidification with concentrated hydrochloric acid
  6. customgave a solid which
  7. customwas then triturated with ether
  8. customto yield beige crystals
  9. customVacuum drying (0.1 Torr) under refluxing toluene for 15 hours
  10. customfollowed by recrystallization from ethanol
  11. customprovided
  12. dry with materialupon drying 1.50 g of colorless crystals, m.p. 186°-188°

出典と根拠

ORDレコード
ord-dbebbed5883b4b1182f4851ac51d87d6
出典データセット
uspto-grants-1984_10
特許番号
US04476311

反応ノート

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