1,4-Dioxane → 1-(4-Chlorobenzoyl)piperazine

HRID 1361484

反応式

HRID 1361484 の反応式
C(OC([N:8]1[CH2:13][CH2:12][N:11]([C:14](=[O:22])[C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.O1CCOCC1>C(Cl)Cl>[Cl:21][C:18]1[CH:17]=[CH:16][C:15]([C:14]([N:11]2[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)=[O:22])=[CH:20][CH:19]=1

参加物

4

反応物 2

HCID 312751,4-DioxaneHCID 49814251tert-Butyl 4-(4-chlorobenzoyl)piperazine-1-carboxylate

生成物 1

HCID 41014841-(4-Chlorobenzoyl)piperazine収率 99%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

4-(4-Chloro-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester (26 g) was dissolved in CH2Cl2 (350 mL). 4M HCL/Dioxane (150 mL) was added. The mixture was stirred at RT for 4 h. White precipitate was formed. The mixture was concentrated. The white solid was washed with Et2O. After the white solid was treated with 1N NaOH (200 mL) and extracted with Ethyl acetate (3×100 mL), the combined organic phase was dried over Na2SO4 and concentrated to give 17.79 g of desired product (99% yield). 1H-NMR (for HCl salt) (300 MHz, MeOD): δ 2.80-2.90 (m, 4 H), 3.20-3.80 (m, 4 H), 7.29-7.36 (m, 4 H).

後処理

  1. customWhite precipitate was formed
  2. concentrationThe mixture was concentrated
  3. washThe white solid was washed with Et2O
  4. additionAfter the white solid was treated with 1N NaOH (200 mL)
  5. extractionextracted with Ethyl acetate (3×100 mL)
  6. dry with materialthe combined organic phase was dried over Na2SO4
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-7f4e8e32b7c6442dbc5d21a19205abd7
出典データセット
uspto-grants-2011_02
特許番号
US07880002B2

関連ノート

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