Triethylamine → HCID 18919916, compound

HRID 1291102Notes

Reaction equation

HRID 1291102 reaction equation
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:22]([C:24]1[CH:32]=[CH:31][C:27]([C:28](Cl)=[O:29])=[CH:26][CH:25]=1)#[N:23]>C1(C)C=CC=CC=1>[C:22]([C:24]1[CH:32]=[CH:31][C:27]([C:28]([O:14][CH:11]2[CH2:12][CH2:13][N:8]([CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH2:9][CH2:10]2)=[O:29])=[CH:26][CH:25]=1)#[N:23]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 784611-Benzylpiperidin-4-olHCID 801724-Cyanobenzoyl chloride

Product 1

HCID 18919916HCID 18919916, compoundYield 61.4%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

2.0 g (0.01 mol) of 1-benzyl-4-hydroxypiperidine and 1.4 ml (0.01 mol) of triethylamine were dissolved in 100 ml of toluene and treated with 1.6 g (0.00966 mol) of 4-cyanobenzoyl chloride. The mixture was boiled at reflux for 2 hrs., the precipitate was filtered off and the filtrate was concentrated. The residue was chromatographed over silica gel with ethyl acetatelhexane (1:1). 1.9 g (61%) of 1-benzyl-piperidin-4-yl 4-cyano-benzoate were obtained as brownish crystals; m.p. 110°-111°.

Workup

  1. temperatureat reflux for 2 hrs
  2. filtration, the precipitate was filtered off
  3. concentrationthe filtrate was concentrated
  4. customThe residue was chromatographed over silica gel with ethyl acetatelhexane (1:1)

Sources & evidence

ORD record
ord-9e94a12ff4214d2faafee013c82038b0
Source dataset
uspto-grants-1998_05
Patent number
US05753679

Reaction notes

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