Camphoric acid, (-)- → HCID 2750589, compound

HRID 645451Notes

Reaction equation

HRID 645451 reaction equation
[C:1](O)(=[O:13])[C@:2]1([CH2:12][CH2:11][C@@H:7]([C:8](O)=[O:9])[C:4]1([CH3:6])[CH3:5])[CH3:3]>C1COCC1.CCOCC>[OH:13][CH2:1][C:2]1([CH3:3])[CH2:12][CH2:11][CH:7]([CH2:8][OH:9])[C:4]1([CH3:6])[CH3:5]

Participants

4

Procedure

To a solution of (1S,3R)-camphoric acid (1) (3.0 g, 14.8 mmol) in dry THF (40 mL) and dry Et2O (30 mL) was added LiALH4 (2.0 g, 52.6 mmol) and the reaction mixture was refluxed for 5 hours. The reaction was then quenched by the addition of Na2SO4.10H2O (8.5 g) and the mixture stirred for 0.5 hour. H2O (100 mL) was added and the aqueous layer extracted with CH2Cl2 (3×50 mL). The combined organic layers were dried over anhydrous MgSO4 and the solvents concentrated in vacuo to a residue which was purified over silica (n-hexane/EtOAc, 6:4) to afford 2.39 g (95% yield) of the desired intermediate (2) as crystals which were characterized as follows:

Workup

  1. temperaturethe reaction mixture was refluxed for 5 hours
  2. customThe reaction was then quenched by the addition of Na2SO4.10H2O (8.5 g)
  3. additionH2O (100 mL) was added
  4. extractionthe aqueous layer extracted with CH2Cl2 (3×50 mL)
  5. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  6. concentrationthe solvents concentrated in vacuo to a residue which
  7. customwas purified over silica (n-hexane/EtOAc, 6:4)

Sources & evidence

ORD record
ord-47732d0fcfc947fb8b270aca852720ac
Source dataset
uspto-grants-2010_04
Patent number
US07704986B2

Reaction notes

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