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

HRID 1594326
Notes
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Reaction equation

HRID 1594326 reaction equation
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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-1c8f2c67c3b84ec5a07f8af0d6f4bfc4
Source dataset
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07300951B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes