Methanol → HCID 18919782, compound

HRID 1291084Notes

Reaction equation

HRID 1291084 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:21]=[CH:22][CH:23]=1)[C:5]([O:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=[O:6].CO>CCOCC>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH:21]=[CH:22][CH:23]=1)[C:5]([O:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:10][CH2:9]1)=[O:6]

Participants

4

Reactant 2

HCID 887MethanolHCID 18919783HCID 18919783, compound

Product 1

HCID 18919782HCID 18919782, compoundYield 172.9%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

0.1 g (0.0003 mol) of 1-benzyl-piperidin-4-yl 3-chloro-benzoate was dissolved in 5 ml of ether and 0.5 ml of methanol and treated with 1 ml of 1N ethereal HCI. The mixture was stirred for 2 hrs. and the resulting precipitate was filtered off, washed with ether and dried. 0.095 g (86%) of 1-benzyl-piperidin-4-yl 3-chloro-benzoate hydrochloride (1:1) was obtained as white crystals, m.p. 212°-213°.

Workup

  1. filtrationand the resulting precipitate was filtered off
  2. washwashed with ether
  3. customdried

Sources & evidence

ORD record
ord-efe8d3556c774342949dfb8df30c0c6e
Source dataset
uspto-grants-1998_05
Patent number
US05753679

Reaction notes

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