1-Pentyne → HCID 59657497, compound

HRID 2055424Notes

Reaction equation

HRID 2055424 reaction equation
[CH:1]#[C:2][CH2:3][CH2:4][CH3:5].C([Li])CCC.[CH2:11]([N:18]1[CH2:23][CH2:22][C:21](=[O:24])[CH2:20][CH2:19]1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1COCC1>[CH2:11]([N:18]1[CH2:23][CH2:22][C:21]([C:1]#[C:2][CH2:3][CH2:4][CH3:5])([OH:24])[CH2:20][CH2:19]1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1

Participants

5

Conditions

Temperature
0 °C

Procedure

To a solution of 5.47 g (80.3 mmol) of 1-pentyne in 65 mL THF at −78° C. was added 32.1 ml n-butyl lithium (80.3 mmol; 2.5M in hexanes). After the addition was complete the reaction mixture was warmed to 0° C. and a solution of 8.44 g (44.6 mmol) of 1-benzyl-4-piperidone and 40 mL of THF was added dropwise. The cooling bath was removed and the reaction mixture was stirred at ambient temperature. After 17 h, the reaction was quenched by addition of saturated ammonium chloride and diluted with EtOAc. The aqueous phase was extracted twice with EtOAc. The combined organic phases were washed with brine, dried over sodium sulfate and evaporated to afford a reddish-gold oil. The crude product was purified by flash chromatography on silica gel (EtOAc/hexane 1:1→65:35). The light gold oil was dried over sodium sulfate to afford 8.91 g (78%) of 1-benzyl-4-pentynyl-4-piperidinol: ms (EST) [M+H]+=258.

Workup

  1. additionAfter the addition
  2. customThe cooling bath was removed
  3. customthe reaction was quenched by addition of saturated ammonium chloride
  4. additiondiluted with EtOAc
  5. extractionThe aqueous phase was extracted twice with EtOAc
  6. washThe combined organic phases were washed with brine
  7. dry with materialdried over sodium sulfate
  8. customevaporated
  9. customto afford a reddish-gold oil
  10. customThe crude product was purified by flash chromatography on silica gel (EtOAc/hexane 1:1→65:35)
  11. dry with materialThe light gold oil was dried over sodium sulfate

Sources & evidence

ORD record
ord-942003b67d9348249b10dcfe65838a2f
Source dataset
uspto-grants-2008_02
Patent number
US07332500B2

Reaction notes

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