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Chlorotrimethylsilane → 2-Amino-4,4,4-trifluorobutan-1-ol

HRID 1594326
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HRID 1594326 반응식
C[Si](Cl)(C)C.[BH4-].[Li+].[NH2:8][CH:9]([CH2:13][C:14]([F:17])([F:16])[F:15])[C:10](O)=[O:11]>C1COCC1>[NH2:8][CH:9]([CH2:13][C:14]([F:17])([F:16])[F:15])[CH2:10][OH:11]
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참가 물질

5

반응물 3

HCID 6397ChlorotrimethylsilaneHCID 3530832-Amino-4,4,4-trifluorobutanoic acidHCID 4148881Lithium borohydride

생성물 1

HCID 534164332-Amino-4,4,4-trifluorobutan-1-ol수율 38.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of trimethylsilyl chloride (1.38 g, 12.73 mmol) was added to a solution of lithium borohydride (3.2 mL, 2.0 M in THF) and THF (5 mL) at 25° C. After stirring 5 min, 2-amino-4,4,4-trifluoro-butyric acid (0.50 g, 3.18 mmol) was added portionwise over a 5 min period. The reaction was allowed to stir 48 h. The reaction was quenched by cautious addition of MeOH (5 mL) dropwise. The solvent was evaporated and the residue treated with potassium hydroxide (KOH) solution (20%, 6 mL). The aqueous phase was extracted using dichloromethane, 3 times (10 mL each). The organic phases were combined and dried over anhydrous sodium sulfate. After filtration the solvent was evaporated to afford the 2-amino-4,4,4-trifluoro-butan-1-ol as an oil (0.174 g, 38%). This oil was used directly in the next reaction without further purification.

후처리

  1. stirringto stir 48 h
  2. customThe reaction was quenched by cautious addition of MeOH (5 mL) dropwise
  3. customThe solvent was evaporated
  4. additionthe residue treated with potassium hydroxide (KOH) solution (20%, 6 mL)
  5. extractionThe aqueous phase was extracted
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationAfter filtration the solvent
  8. customwas evaporated

출처 및 근거

ORD 기록
ord-1c8f2c67c3b84ec5a07f8af0d6f4bfc4
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07300951B2

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