4-cyclopentylpentanoic acid → HCID 22476837, compound

HRID 2187314Notes

Reaction equation

HRID 2187314 reaction equation
[CH:1]1([CH:6]([CH3:12])[CH2:7][CH2:8][C:9](O)=[O:10])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(OCC)C.C1COCC1>[CH:1]1([CH:6]([CH3:12])[CH2:7][CH2:8][CH2:9][OH:10])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

5

Procedure

A solution of 4-cyclopentylpentanoic acid (16 g; 94 mmol) in diethyl ether (30 ml) and THF (30 ml) was added within 20 minutes to lithium aluminum hydride (3.6 g; 94 mmol) and suspended in the same solvent (100 ml). After 2 hours at reflux, the reaction mixture was cooled with an ice-bath and quenched successively with water (4 ml), 15% sodium hydroxide (12 ml) and again water (4 ml). The white solid was filtered off, and the mixture diluted with MTBE (300 ml), washed with 1 N HCl (300 ml), sodium bicarbonate solution (300 ml) and brine (2×300 ml), dried (MgSO4), concentrated in vacuo, and distilled (59° C./0.075 torr) to give 8.7 g (59% yield) of 4-cyclopentylpentan-1-ol.

Workup

  1. temperatureAfter 2 hours at reflux
  2. temperaturethe reaction mixture was cooled with an ice-bath
  3. customquenched successively with water (4 ml), 15% sodium hydroxide (12 ml) and again water (4 ml)
  4. filtrationThe white solid was filtered off
  5. additionthe mixture diluted with MTBE (300 ml)
  6. washwashed with 1 N HCl (300 ml), sodium bicarbonate solution (300 ml) and brine (2×300 ml)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo
  9. distillationdistilled (59° C./0.075 torr)

Sources & evidence

ORD record
ord-3079c94baf7b4dfc93e040c9ce3b4c7e
Source dataset
uspto-grants-2002_06
Patent number
US06410000B1

Reaction notes

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