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Hydrochloric Acid → HCID 67593614、化合物

HRID 1379144
ノート
印刷プレビュー

反応式

HRID 1379144 の反応式
[Cl:1][CH:2]1[S:7][C:6]2[S:8][CH:9]=[CH:10][C:5]=2[C:4](=[O:11])[CH2:3]1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[F:22][C:23]([F:32])([F:31])[C:24](C1NC=CN=1)=[O:25].Cl>O1CCCC1>[Cl:1][CH:2]1[S:7][C:6]2[S:8][CH:9]=[C:10]([C:24](=[O:25])[C:23]([F:32])([F:31])[F:22])[C:5]=2[C:4](=[O:11])[CH2:3]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 5654362,2,2-Trifluoro-1-(1H-imidazol-2-yl)ethanoneHCID 2724254Sodium bis(trimethylsilyl)amideHCID 67594742HCID 67594742、化合物

生成物 1

HCID 67593614HCID 67593614、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

The compound from Step 3 (1.03 g, 5.0 mmol) was dissolved in tetrahydrofuran (50 mL) and cooled to -78° C. A solution of sodium bistrimethylsilylamide (5.0 mL of a 1.0M tetrahydrofuran solution) was added and the reaction stirred for 0.75 hours at -78° C. Trifluoroacetyl imidazole (0.68 mL, 6.0 mmol) was added and the reaction was warmed to room temperature and stirred under a nitrogen atmosphere for 16 hours. At this time, 1N hydrochloric acid (300 mL) was added to the reaction followed by extraction with ether (350 mL). The organics were washed with brine (200 mL), dried over MgSO4 and concentrated in vacuo. The resulting yellow oil was used without further purification.

後処理

  1. temperaturethe reaction was warmed to room temperature
  2. stirringstirred under a nitrogen atmosphere for 16 hours
  3. extractionfollowed by extraction with ether (350 mL)
  4. washThe organics were washed with brine (200 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe resulting yellow oil was used without further purification

出典と根拠

ORDレコード
ord-8369ff7ab4224ac68cfed2dc6fd54adf
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05670532

反応ノート

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