Bromine → 1-Acetamido-4-bromo-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthalene

HRID 863522ノート

反応式

HRID 863522 の反応式
[C:1]([NH:4][C:5]1[C:14]2[CH2:13][CH:12]([N:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)[CH2:11][CH2:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)(=[O:3])[CH3:2].O.O.O.C([O-])(=O)C.[Na+].[Br:28]Br>C(O)(=O)C>[C:1]([NH:4][C:5]1[C:14]2[CH2:13][CH:12]([N:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)[CH2:11][CH2:10][C:9]=2[C:8]([Br:28])=[CH:7][CH:6]=1)(=[O:3])[CH3:2]

参加物

5

反応物 3

HCID 24408BromineHCID 196962461-Acetamido-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthaleneHCID 23665404Sodium Acetate Trihydrate

生成物 1

HCID 196962081-Acetamido-4-bromo-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthalene

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A solution of 1-acetamido-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthalene (0.36 g, 1.4 mmol) and sodium acetate trihydrate (0.38 g, 2.8 mmol) in acetic acid (15 mL) was treated with bromine (0.27 g, 1.7 mmol) and stirred at room temperature for 2 h. A precipitate was collected by filtration and the filtrate evaporated. The two solids were combined and dissolved in methylene chloride; water. The mixture was basified with 12.5% NaOH, and the organic phase separated. The aqueous layer was back extracted and the combined organic layers were dried over sodium sulfate, filtered and evaporated. The residue was heated in diethyl ether to form a solid, which was collected and dried (0.31 g).

後処理

  1. filtrationA precipitate was collected by filtration
  2. customthe filtrate evaporated
  3. dissolutiondissolved in methylene chloride
  4. customthe organic phase separated
  5. extractionThe aqueous layer was back extracted
  6. dry with materialthe combined organic layers were dried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. temperatureThe residue was heated in diethyl ether
  10. customto form a solid, which
  11. customwas collected
  12. customdried (0.31 g)

出典と根拠

ORDレコード
ord-6a6d7991919f49c697e7ed58b5f3c16f
出典データセット
uspto-grants-1998_02
特許番号
US05721234

反応ノート

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