Hydrochloric Acid → HCID 18678400, compound
Reaction equation
[CH3:1][O:2][CH:3]([O:20][CH3:21])[CH:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:19]=[CH:18][C:13]([C:14]([O:16]C)=[O:15])=[CH:12][CH:11]=2)[CH2:6][CH2:5]1.Cl>CO>[CH3:1][O:2][CH:3]([O:20][CH3:21])[CH:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:19]=[CH:18][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=2)[CH2:6][CH2:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A solution of methyl 4-(4-(dimethoxymethyl)piperidinyl)benzoate(5.6 g, 18.2 mol) was in methanol (50 mL) 1N sodium hydroxide (27 mL) was heated at 80° C. for 5 hours. The reaction was neutralized with 1N HCl (27 ml) and concentrated in vacuo. Additional methanol was added to the residue which was filtered (0.5 micron filter) and evaporated to give 5.0 g of the product.
Workup
- concentrationconcentrated in vacuo
- additionAdditional methanol was added to the residue which
- filtrationwas filtered
- filtration(0.5 micron filter)
- customevaporated
Sources & evidence
- ORD record
- ord-51422a2766a04a949af58d559798cf72
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506901B2
Reaction notes
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