HCID 9834575, compound → HCID 9833987, compound

HRID 1797393Notes

Reaction equation

HRID 1797393 reaction equation
C([O:8][CH2:9][CH2:10][C@H:11]([OH:17])[C:12]([CH3:16])([CH3:15])[C:13]#[N:14])C1C=CC=CC=1>[OH-].[OH-].[Pd+2].O1CCCC1>[OH:8][CH2:9][CH2:10][C@H:11]([OH:17])[C:12]([CH3:16])([CH3:15])[C:13]#[N:14]

Participants

4

Reactant 1

HCID 9834575HCID 9834575, compound2×

Product 1

HCID 9833987HCID 9833987, compound

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 8028TetrahydrofuranSolvent

Procedure

16 g of Pearlman's catalyst (Pd(OH)2 on carbon, 20%) is added to 11.13 g (47.70 mmol) of 5-benzyloxy-2,2-dimethyl-3(S)-hydroxy-pentane-nitrile of the title compound of Example 1c, dissolved in 110 ml of tetrahydrofuran. It is now hydrogenated for 7.5 hours at 10 bar and at room temperature. Catalyst is filtered out, and the filtrate is evaporated to the dry state in a vacuum.

Workup

  1. filtrationCatalyst is filtered out
  2. customthe filtrate is evaporated to the dry state in a vacuum

Sources & evidence

ORD record
ord-d771bd97d0b1442f9a5d4a7d491a8de9
Source dataset
uspto-grants-2006_04
Patent number
US07034165B2

Reaction notes

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