HCID 22841026, compound → HCID 22841028, compound

HRID 329513Notes

Reaction equation

HRID 329513 reaction equation
C([O:8][CH2:9][C@H:10]1[C@H:15]([O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:14][CH2:13][CH2:12][O:11]1)C1C=CC=CC=1.[H][H]>[Pd].CO>[CH2:17]([O:16][C@@H:15]1[CH2:14][CH2:13][CH2:12][O:11][C@H:10]1[CH2:9][OH:8])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]

Participants

5

Reactant 2

HCID 22841026HCID 22841026, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 22841028HCID 22841028, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

1.5 g of 10% w/w palladium on activated carbon was added to a solution of 3.757 g of dl-trans-2-benzyloxymethyl-3-hexadecyloxytetrahydropyran (prepared as described in Preparation 43) in 150 ml of methanol, and the whole was mixed with hydrogen by shaking in a Paar's apparatus at room temperature under a pressure of 4 atmospheres (about 4 bars). After 20 hours, the catalyst was removed by filtration, and the solvent was then removed by distillation to give 2.749 g of the title compound as a solid, melting at 41°-42° C. (after recrystallization from cold hexane).

Workup

  1. customthe catalyst was removed by filtration
  2. customthe solvent was then removed by distillation
  3. customto give
  4. custom2.749 g of the title compound as a solid, melting at 41°-42° C. (after recrystallization from cold hexane)

Sources & evidence

ORD record
ord-adb8d3ea31b3421389b75a0f745c4a09
Source dataset
uspto-grants-1990_01
Patent number
US04891363

Reaction notes

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