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2-Chlorophenol → 1-Benzyl-4-(4-methoxybenzylidene)-piperidine

HRID 895463
Notes
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Reaction equation

HRID 895463 reaction equation
C(OC(N1CC[CH:11]([O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2Cl)CC1)=O)(C)(C)C.C(O[C:27]([N:29]1[CH2:34][CH2:33][CH:32](O)[CH2:31][CH2:30]1)=O)(C)(C)C.Cl[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=1O.[C:44]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C>CCOC(C)=O>[CH2:27]([N:29]1[CH2:30][CH2:31][C:32](=[CH:44][C:18]2[CH:17]=[CH:16][C:15]([O:14][CH3:11])=[CH:20][CH:19]=2)[CH2:33][CH2:34]1)[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 72452-ChlorophenolHCID 11776TriphenylphosphineHCID 643502Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 5363146Diisopropyl azodicarboxylateHCID 16732586Tert-butyl 4-(2-chlorophenoxy)piperidine-1-carboxylate

Product 1

HCID 22378870
1-Benzyl-4-(4-methoxybenzylidene)-piperidine

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

4-(2-Chlorophenoxy)-piperidine-1-carboxylic acid tert-butyl ester (10.6) This compound was prepared from 4-hydroxypiperidine-1-carboxylic acid tert-butyl ester (9) (3.505 g; 17.4 mmol), 2-chloro-phenol (3.375 g; 26.3 mmol), triphenylphosphine (6.002 g; 22.9 mmol) and DIAD (4.30 mL; 21.8 mmol) in a manner analogous to 10.5. After 8 days, EtOAc (200 mL) was added to the crude reaction mixture and the solution washed with 50% saturated NaHCO3 (50 mL), saturated NaHCO3 (2×25 mL) and saturated NaCl (2×25 mL) then dried (MgSO4), filtered and concentrated to a viscous liquid. Ether (50 mL) and hexanes (50 mL) were added and this was allowed to stand overnight; whereupon the precipitate was removed by filtration and the filtrate partially concentrated. More material precipitated, which was also removed by filtration, and the filtrate was concentrated to an oil. The product was partially purified on basic alumina (160 mL), eluting with 8:1 hexanes:EtOAc, giving a clear, colorless viscous liquid (5.12 g; 94% crude yield). LC (method A) tR=11.50 min; ESIMS 312.1/314.1 (1/0.3) [MH+], 296.9/298.9 (100/34) [MH+−C4H9+CH3CN], 255.9/257.8 (41/12) [MH+−C4H9], 212.0/214.0 (4/1) [MH+−C4H9−CO2]

Workup

  1. customreaction mixture
  2. washthe solution washed with 50% saturated NaHCO3 (50 mL), saturated NaHCO3 (2×25 mL) and saturated NaCl (2×25 mL)
  3. dry with materialthen dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated to a viscous liquid
  6. additionEther (50 mL) and hexanes (50 mL) were added
  7. waitto stand overnight
  8. customwhereupon the precipitate was removed by filtration
  9. concentrationthe filtrate partially concentrated
  10. customMore material precipitated
  11. customwhich was also removed by filtration
  12. concentrationthe filtrate was concentrated to an oil
  13. customThe product was partially purified on basic alumina (160 mL)
  14. washeluting with 8:1 hexanes
  15. customEtOAc, giving a clear, colorless viscous liquid (5.12 g; 94% crude yield)

Sources & evidence

ORD record
ord-31bfcc6e231d426eb370313a1463bff3
Source dataset
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06916804B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes