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Tributylstannane → 3-(Perfluoroisopropyl)propanol

HRID 548531
Notes
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Reaction equation

HRID 548531 reaction equation
[F:1][C:2]([C:12]([F:15])([F:14])[F:13])([C:8]([F:11])([F:10])[F:9])[CH2:3][CH:4](I)[CH2:5][OH:6].C([SnH](CCCC)CCCC)CCC>>[F:1][C:2]([C:12]([F:13])([F:14])[F:15])([C:8]([F:9])([F:11])[F:10])[CH2:3][CH2:4][CH2:5][OH:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 5948TributylstannaneHCID 27826014,5,5,5-Tetrafluoro-2-iodo-4-(trifluoromethyl)pentan-1-ol

Product 1

HCID 5427393-(Perfluoroisopropyl)propanol

Procedure

In accordance with scheme (9) above, a 500 mL two neck round bottom flask can be equipped with a thermocouple, agitator, and heating mantle. About 212.1 g (0.599 mole) 4,5,5,5-tetrafluoro-4(trifluoromethyl)-2-iodopentan-1-ol (212.1 g, 0.599 mole) can be added to the flask and heated to about 60° C. to 70° C. From a 100 mL pressure equalized addition funnel, about 196.4 g (0.675 mole) tributyltin hydride can be added drop-wise over a 4 hour period followed by 2 hours of continued heating and stirring. The RF-intermediate 4,5,5,5-tetrafluoro-4(trifluoromethyl)pentan-1-ol, can be obtained through vacuum distillation and verified by gas chromatography/mass spectrometry (m/z 228 (M+), 211 (M+-OH), 159 (M+-CF3)).

Workup

  1. temperature
heating mantle
  • temperatureheated to about 60° C. to 70° C
  • additionaddition funnel
  • temperatureof continued heating
  • Sources & evidence

    ORD record
    ord-c21c70b82d7e4153954dd9fa9f622203
    Source dataset
    uspto-grants-2011_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07943567B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes