Hydrochloric Acid → Piperazic acid t-butyl ester dihydrochloride salt

HRID 542746

反応式

HRID 542746 の反応式
S(=O)(=O)(O)O.[N:6]1([C:12]([OH:14])=[O:13])[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1.[CH3:15][C:16](=[CH2:18])[CH3:17].[OH-].[Na+].[ClH:21]>CCOCC.O1CCOCC1>[ClH:21].[ClH:21].[C:16]([O:13][C:12]([N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:14])([CH3:18])([CH3:17])[CH3:15]

参加物

8

実験手順

A 250 ml pyrex heavy-walled pressure bottle is charged with 50 ml of dioxane, 3 ml of concentrated sulfuric acid, 1.3 g (0.01 mole) of piperazic acid (II-A) and approximately 75 ml of isobutylene, liquified by passage into a large test-tube cooled in a dry ice-acetone bath. The bottle is closed with a rubber stopper, clamped securely in place, and is shaken mechanically at room temperature overnight. The bottle is chilled in an ice bath and opened. The contents are poured into a separatory funnel containing a cold mixture of 200 ml of ether and 125 ml of 1N sodium hydroxide. The aqueous layer is washed with ether. The combined ethereal solution is dried over sodium sulfate and evaporated under vacuum to afford an oil, which is dissolved in 25 ml of ether. Addition of dry hydrogen chloride gives 1.3 g of crystalline piperazic acid t-butyl ester dihydrochloride salt (II-B).

後処理

  1. customliquified by passage into a large test-tube
  2. temperaturecooled in a dry ice-acetone bath
  3. customThe bottle is closed with a rubber stopper
  4. temperatureThe bottle is chilled in an ice bath
  5. additionThe contents are poured into a separatory funnel
  6. additioncontaining
  7. washThe aqueous layer is washed with ether
  8. dry with materialThe combined ethereal solution is dried over sodium sulfate
  9. customevaporated under vacuum
  10. customto afford an oil, which

出典と根拠

ORDレコード
ord-6e44bd37e4854f49b1d4695524679ea3
出典データセット
uspto-grants-1987_04
特許番号
US04659711

関連ノート

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