Benzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylate → HCID 49760816, compound

HRID 1692271Notes

Reaction equation

HRID 1692271 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH3:25])=[C:6]([CH:8]2[CH2:13][CH2:12][N:11](C(OCC3C=CC=CC=3)=O)[CH2:10][CH2:9]2)[CH:7]=1>Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH3:25])=[C:6]([CH:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[CH:7]=1

Participants

3

Procedure

A solution of benzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylate (Preparation 234, 73 g, 0.2 mol) in concentrated hydrochloric acid (200 ml) was refluxed with stirring for 2 hours before concentrating in vacuo. Water (100 ml), sodium hydroxide (10 M aqueous solution, 20 ml) and chloroform (200 ml) were added to the residue. The aqueous layer was extracted with chloroform (2×200 ml). The combined organic layers were washed with water (200 ml), saturated aqueous sodium chloride solution (200 ml), dried over sodium sulphate, filtered through silica gel (100 g, 40/63 μm) and evaporated in vacuo to afford the title compound as white crystals, 40 g, 89% yield.

Workup

  1. concentrationbefore concentrating in vacuo
  2. additionWater (100 ml), sodium hydroxide (10 M aqueous solution, 20 ml) and chloroform (200 ml) were added to the residue
  3. extractionThe aqueous layer was extracted with chloroform (2×200 ml)
  4. washThe combined organic layers were washed with water (200 ml), saturated aqueous sodium chloride solution (200 ml)
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered through silica gel (100 g, 40/63 μm)
  7. customevaporated in vacuo

Sources & evidence

ORD record
ord-79bc94f07bb143d7816d7be7b9eaa631
Source dataset
uspto-grants-2012_04
Patent number
US08153814B2

Reaction notes

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