Sodium Fluoride → HCID 67198384, compound

HRID 551653Notes

Reaction equation

HRID 551653 reaction equation
[CH:1]1([CH:6]([CH2:12][CH:13]=[CH2:14])[C:7](OCC)=[O:8])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[F-].[Na+]>O1CCCC1.O.C(OCC)(=O)C>[CH:1]1([CH:6]([CH2:12][CH:13]=[CH2:14])[CH2:7][OH:8])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

7

Conditions

Temperature
0 °C

Procedure

A tetrahydrofuran (15 mL) solution of ethyl 2-cyclopentylpent-4-enoate (6.10 g, 31.6 mmol) was added dropwise over 20 minutes to a tetrahydrofuran (40 mL) solution of lithium aluminum hydride (1.21 g, 31.9 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 (14.0 mL), water (11.3 mL), tetrahydrofuran (21.0 mL), and sodium fluoride (13.4 g) were added thereto, and the mixture was stirred for 1 hour. 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 (3.50 g, 56%).

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 hour
  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 (3.50 g, 56%)

Sources & evidence

ORD record
ord-271a04fc3141494297ff324161a3086f
Source dataset
uspto-grants-2011_05
Patent number
US07947738B2

Reaction notes

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