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Hydrochloric Acid → HCID 67593614, 화합물

HRID 1419086
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HRID 1419086 반응식
[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
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참가 물질

6

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

생성물 1

HCID 67593614HCID 67593614, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-78 °C

실험 절차

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 vacua. The resulting yellow oil was used without further purification.

후처리

  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 vacua
  7. customThe resulting yellow oil was used without further purification

출처 및 근거

ORD 기록
ord-cdb45857f92a4d7386a5ba9b631d46a5
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05886016

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