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Sodium → HCID 69658454、化合物

HRID 2212969
ノート
印刷プレビュー

反応式

HRID 2212969 の反応式
[Na].[CH2:2]([O:4][C:5]([C@@H:7]1[CH2:11][CH2:10][CH2:9][C@@H:8]1[C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[C:18]([C:21]#[N:22])[CH:19]=2)[NH:14][CH:13]=1)=[O:6])C>CO>[CH3:2][O:4][C:5]([C@@H:7]1[CH2:11][CH2:10][CH2:9][C@H:8]1[C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[C:18]([C:21]#[N:22])[CH:19]=2)[NH:14][CH:13]=1)=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5360545SodiumHCID 69658351HCID 69658351、化合物

生成物 1

HCID 69658454HCID 69658454、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

Sodium metal (13.5 g, 556 mMol) was carefully added portion-wise to anhydrous methanol (400 mL). A solution of cis-2-(5-cyanoindol-3-yl)-cyclopentanecarboxylic acid ethyl ester (33.1 g, 117 mMol) in methanol (100 mL) was added over 5 minutes. The mixture was heated at a gentle reflux for 18 hours, carefully quenched with water, and evaporated in vacuo. The residue was dissolved ethyl acetate (600 mL), washed with saturated sodium chloride (100 mL), dried over sodium sulfate, and concentrated in vacuo to give the product as an 88:12 cis/trans diastereomeric mixture which was used without further purification (27 g, 86%).

後処理

  1. temperatureThe mixture was heated at
  2. temperaturea gentle reflux for 18 hours
  3. customcarefully quenched with water
  4. customevaporated in vacuo
  5. dissolutionThe residue was dissolved ethyl acetate (600 mL)
  6. washwashed with saturated sodium chloride (100 mL)
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated in vacuo
  9. customto give the product as an 88:12 cis/trans diastereomeric mixture which
  10. customwas used without further purification (27 g, 86%)

出典と根拠

ORDレコード
ord-6aed4c6f273e4ab68f4d3c79db84bba7
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105516B2

反応ノート

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