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Ethyl ketone → HCID 18187644, compound

HRID 278264
Notes
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Reaction equation

HRID 278264 reaction equation
C(NC(C)C)(C)C.C([Li])CCC.[CH3:13][CH2:14][C:15](=[O:18])[CH2:16][CH3:17].[C:19]([O:23][C:24]([N:26]1[CH2:31][CH2:30][CH:29]([CH:32]=[O:33])[CH2:28][CH2:27]1)=[O:25])([CH3:22])([CH3:21])[CH3:20]>C1COCC1>[C:19]([O:23][C:24]([N:26]1[CH2:31][CH2:30][CH:29]([CH:32]([OH:33])[CH:14]([CH3:13])[C:15](=[O:18])[CH2:16][CH3:17])[CH2:28][CH2:27]1)=[O:25])([CH3:22])([CH3:21])[CH3:20]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 7288Ethyl ketoneHCID 7912DiisopropylamineHCID 1514430tert-Butyl 4-formylpiperidine-1-carboxylateHCID 178418339Butyllithium

Product 1

HCID 18187644HCID 18187644, compoundYield 85%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent
2×

Conditions

Temperature
0 °C

Procedure

A solution of diisopropylamine (0.63 mL, 4.5 mmol) in THF (16 mL) at 0° C. was treated with 1.6 M n-butyllithium in sol'n in hexanes (2.8 mL). The resulting solution was stirred at 0° C. for 10 min, then cooled to −78° C. 3-Pentanone (0.41 mL, 4.1 mmol) was added and the resulting mixture was stirred cold for 1 h. A solution of 1-(t-butoxycarbonyl)-4-formylpiperidine (435 mg, 2.05 mmol) (from Step B) in THF (3 mL) was then added. After 15 min, the reaction was quenched with sat'd ammonium chloride (25 mL) and extracted with ether (100 mL). The extract was dried over magnesium sulfate and concentrated. MPLC (Biotage) on a 40S silica cartridge using 4:1 v/v, then 3:2 v/v hexanes/ethyl acetate as the eluent afforded 517 mg (85%) of the title compound.

Workup

  1. temperaturecooled to −78° C
  2. stirringthe resulting mixture was stirred cold for 1 h
  3. waitAfter 15 min
  4. customthe reaction was quenched with sat'd ammonium chloride (25 mL)
  5. extractionextracted with ether (100 mL)
  6. dry with materialThe extract was dried over magnesium sulfate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-63dc8522428a4c128ae145b14f6853a9
Source dataset
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06358979B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes