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Methyl iodide → 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester

HRID 1641775
Notes
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Reaction equation

HRID 1641775 reaction equation
[CH3:1][O:2][C:3](=[O:19])[CH2:4][CH2:5][CH:6]1[CH2:11][CH2:10][N:9]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:8][CH2:7]1.[CH3:20][Si]([N-][Si](C)(C)C)(C)C.[Na+].CI>O1CCCC1>[CH3:1][O:2][C:3](=[O:19])[CH:4]([CH3:20])[CH2:5][CH:6]1[CH2:11][CH2:10][N:9]([C:12]([O:14][C:15]([CH3:16])([CH3:18])[CH3:17])=[O:13])[CH2:8][CH2:7]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 1502093Methyl N-Boc-4-piperidinepropionateHCID 2724254Sodium bis(trimethylsilyl)amide

Product 1

HCID 592610702-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester (2.0 g, 7.38 mmol) from above was dissolved in tetrahydrofuran (50 mL). The solution was cooled to −78° C. and sodium bis(trimethylsilyl)amide (1.0 M, 9.0 mL) was added. The mixture was stirred at −78° C. for 1 hr and methyl iodide (1.2 mL, 19.5 mmol) was added. The mixture was warmed to room temperature and stirred for 2 hrs. The mixture was extracted with ether and washed with dilute hydrochloric acid. The organic layer was dried, filtered and concentrated. The residue was purified using flash chromatography (eluting with ethyl acetate and hexanes) to give 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester as an oil (789 mg).

Workup

  1. temperatureThe mixture was warmed to room temperature
  2. stirringstirred for 2 hrs
  3. extractionThe mixture was extracted with ether
  4. washwashed with dilute hydrochloric acid
  5. customThe organic layer was dried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified
  9. washflash chromatography (eluting with ethyl acetate and hexanes)

Sources & evidence

ORD record
ord-44587313d66a4a58b9933e8e615839e6
Source dataset
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08115011B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes