Sodium Hydroxide → HCID 15045342, compound

HRID 1769669Notes

Reaction equation

HRID 1769669 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][O:8][C:9]1[CH:10]=[C:11]([CH2:17][C:18]([N:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH:21]2[C:26](OC)=[O:27])=O)[CH:12]=[CH:13][C:14]=1[O:15][CH3:16].[OH-].[Na+].S([O-])([O-])(=O)=O.[Mg+2]>O1CCCC1.O.C(OCC)(=O)C>[CH3:7][O:8][C:9]1[CH:10]=[C:11]([CH2:17][CH2:18][N:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH:21]2[CH2:26][OH:27])[CH:12]=[CH:13][C:14]=1[O:15][CH3:16]

Participants

8

Procedure

2.33 g of lithium aluminum hydride was suspended into 50 ml of tetrahydrofuran and stirred. 3.94 g of methyl N-(3,4-dimethoxyphenylacetyl)piperidine-2-carboxylate was dissolved in 20 ml of tetrahydrofuran, which was dropped and, thereafter, refluxed for 30 min. After cooling with ice and decomposing the excess reagent with ethyl acetate, 2.3 ml of water, 2.3 ml of an aqueous 15% solution of sodium hydroxide and 7 ml of water were added successively and, further, anhydrous magnesium sulfate was added and stirred. Insoluble matters were filtered out and the filtrate was washed thoroughly with tetrahydrofuran. The filtrate was concentrated and purified on silica gel column chromatography (solvent: dichloromethane:methanol:concentrated aqueous ammonium=1000:100:2), to obtain 2.77 g of the above-captioned compound as white solid (yield: 81%).

Workup

  1. additionwhich was dropped
  2. temperaturerefluxed for 30 min
  3. temperatureAfter cooling with ice
  4. additionwere added successively
  5. stirringstirred
  6. filtrationInsoluble matters were filtered out
  7. washthe filtrate was washed thoroughly with tetrahydrofuran
  8. concentrationThe filtrate was concentrated
  9. custompurified on silica gel column chromatography (solvent: dichloromethane:methanol:concentrated aqueous ammonium=1000:100:2)

Sources & evidence

ORD record
ord-07ab97cc9602440ab3816b376a4cdefc
Source dataset
uspto-grants-1995_01
Patent number
US05382595

Reaction notes

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