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

HRID 1594326
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Reaktionsgleichung

Reaktionsgleichung von HRID 1594326
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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Komponenten

5

Edukt 3

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

Produkt 1

HCID 534164332-Amino-4,4,4-trifluorobutan-1-olAusbeute 38,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-1c8f2c67c3b84ec5a07f8af0d6f4bfc4
Quelldatensatz
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07300951B2

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