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Hydrochloric Acid → HCID 67593801、化合物

HRID 865308
ノート
印刷プレビュー

反応式

HRID 865308 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7](=[O:13])[CH2:8][S:9][CH2:10]2)=[CH:5][CH:4]=1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[F:24][C:25]([F:34])([F:33])[C:26](C1NC=CN=1)=[O:27].Cl>O1CCCC1>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7](=[O:13])[CH:8]([C:26](=[O:27])[C:25]([F:34])([F:33])[F:24])[S:9][CH2:10]2)=[CH:5][CH:4]=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 3232557-Methoxy-1H-isothiochromen-4(3H)-oneHCID 5654362,2,2-Trifluoro-1-(1H-imidazol-2-yl)ethanoneHCID 2724254Sodium bis(trimethylsilyl)amide

生成物 1

HCID 67593801HCID 67593801、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

7-Methoxyisothiochroman-4-one from Step 3 (0.58 g, 3.0 mmol) was dissolved in tetrahydrofuran (30 mL) and cooled to -78° C. A solution of sodium bistrimethylsilylamide (3.0 mL of a 1.0M tetrahydrofuran solution) was added and the reaction stirred for 0.5 hours at -78° C. Trifluoroacetyl imidazole (0.41 mL, 3.6 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 (200 mL) was added to the reaction followed by extraction with ether (250 mL). The organics were washed with brine (150 mL), dried over MgSO4 and concentrated in vacuo. The resulting yellow oil (0.42 g, 48%) 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 (250 mL)
  4. washThe organics were washed with brine (150 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe resulting yellow oil (0.42 g, 48%) was used without further purification

出典と根拠

ORDレコード
ord-535d7ced92f240aeaa55ce919b9e359f
出典データセット
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05565482

反応ノート

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