Sodium Fluoride → HCID 86646135, compound

HRID 551644Notes

Reaction equation

HRID 551644 reaction equation
[CH:1]([CH:5]([CH2:11][CH:12]=[CH2:13])[C:6](OCC)=[O:7])([CH2:3][CH3:4])[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].[F-].[Na+]>O1CCCC1.O.C(OCC)(=O)C>[CH:1]([CH:5]([CH2:11][CH:12]=[CH2:13])[CH2:6][OH:7])([CH2:3][CH3:4])[CH3:2]

Participants

7

Conditions

Temperature
0 °C

Procedure

A tetrahydrofuran (50 mL) solution of ethyl 2-sec-butylpent-4-enoate was added dropwise over 30 minutes to a tetrahydrofuran (120 mL) solution of lithium aluminum hydride (4.79 g, 126.3 mmol) cooled to 0° C., and the mixture was then stirred at 0° C. for 1 hour and then stirred at room temperature for 2 hours. The mixture was cooled again to 0° C. Ethyl acetate (55.4 mL), water (44.7 mL), tetrahydrofuran (83.1 mL), and sodium fluoride (53.0 g) were added thereto, and the mixture was stirred for 1.5 hours. The mixture was filtered through Celite to remove insoluble matter. Then, the solution was concentrated, and the residue was purified by silica gel column chromatography to obtain the compound of interest as a colorless oil substance (12.20 g, 69%).

Workup

  1. stirringstirred at room temperature for 2 hours
  2. temperatureThe mixture was cooled again to 0° C
  3. stirringthe mixture was stirred for 1.5 hours
  4. filtrationThe mixture was filtered through Celite
  5. customto remove insoluble matter
  6. concentrationThen, the solution was concentrated
  7. customthe residue was purified by silica gel column chromatography
  8. customto obtain the compound of interest as a colorless oil substance (12.20 g, 69%)

Sources & evidence

ORD record
ord-766bc34c8f804b49ab278c55265f5925
Source dataset
uspto-grants-2011_05
Patent number
US07947738B2

Reaction notes

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