Lithium Hydroxide → HCID 10707604, compound
Reaction equation
C([O:3][C:4](=[O:22])/[C:5](/[CH3:21])=[CH:6]/[C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[C:9]([O:15][CH:16]2[CH2:20][CH2:19][CH2:18][CH2:17]2)[CH:8]=1)C.[Li+].[OH-].O.[OH-].[Li+]>CO.O>[CH:16]1([O:15][C:9]2[CH:8]=[C:7](/[CH:6]=[C:5](\[CH3:21])/[C:4]([OH:22])=[O:3])[CH:12]=[CH:11][C:10]=2[O:13][CH3:14])[CH2:17][CH2:18][CH2:19][CH2:20]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of (E)-3-(3-cyclopentoxy-4-methoxyphenyl)-2-methyl-acrylic acid ethyl ester (30 g 98.6 mmol) and LiOH.OH2O (lithium hydroxide hydrate) (5.0 g, 119.2 mmol, 1.2 equiv.) in methanol-water (4:1, 100 mL) was stirred at room temperature for 24 hours. Methanol was removed under reduced pressure and the resulting residue was dissolved in water (100 mL), washed with three 100 mL portions of ethyl acetate, neutralized with 1.0N HCl (hydrochloric acid) (100 mL), and extracted with two 150 mL portions of ethyl acetate. The extract was washed with brine, dried over anhydrous Na2SO4 (sodium sulfate), and concentrated under reduced pressure to afford the desired product as a light yellow powder (18.2 g, 66% yield). 1H NMR (300 MHz, CDCl3) δ (ppm): 12.4 (br. s, 1H, COOH), 7.56 (s, 1H, olefinic), 7.04 (m, 3H, aromatic), 4.81 (m, 1H), 3.78 (s, 3H, OCH3) , 2.06 (s, 3H, CH3), 1.91-1.57 (m, 8H, cyclopentyl).
Workup
- customMethanol was removed under reduced pressure
- dissolutionthe resulting residue was dissolved in water (100 mL)
- washwashed with three 100 mL portions of ethyl acetate
- extractionextracted with two 150 mL portions of ethyl acetate
- washThe extract was washed with brine
- dry with materialdried over anhydrous Na2SO4 (sodium sulfate)
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-6e6ce7354c534c9991c5418117761255
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06455562B1
Reaction notes
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