Potassium Hydroxide → HCID 15052454, compound
Reaction equation
[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH2:15][CH2:16][C:17]([O:19]C)=[O:18])[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-].[K+]>CO.O>[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH2:15][CH2:16][C:17]([OH:19])=[O:18])[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirring solution of 0.38 g (1.37 mmol) of methyl 3-(3-cyclopentoxy-4-methoxyphenyl)-n-propanoate in 20 mL of methanol was added dropwise 25 mL of a 1.0N solution of potassium hydroxide in water over a 5 minute period. The mixture precipitated immediately, but returned to a solution after a 16 hour period at which time the solution was concentrated, diluted with 20 mL of water and neutralized to pH 1.0 with concentrated hydrochloric acid. The analytically pure white solid which formed was collected, washed several times with cold water, and dried in vacuo.
Workup
- customThe mixture precipitated immediately
- concentrationthe solution was concentrated
- additiondiluted with 20 mL of water and neutralized to pH 1.0 with concentrated hydrochloric acid
- customThe analytically pure white solid which formed
- customwas collected
- washwashed several times with cold water
- customdried in vacuo
Sources & evidence
- ORD record
- ord-dc28e03923f443dd9847a349094b37d9
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05274002
Reaction notes
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