1-(Chloromethoxy)-2-methoxyethane → (E)-6-[1,3-Dihydro-6-methoxy-4-[(2-methoxyethoxy)methoxy]-7-methyl-3-oxo-5-isobenzofuranyl]-4-methyl-4-hexenoic Acid Methyl Ester
Reaction equation
[OH:1][C:2]1[C:10]([CH2:11]/[CH:12]=[C:13](\[CH3:20])/[CH2:14][CH2:15][C:16]([O:18][CH3:19])=[O:17])=[C:9]([O:21][CH3:22])[C:8]([CH3:23])=[C:7]2[C:3]=1[C:4](=[O:24])[O:5][CH2:6]2.C(N(C(C)C)CC)(C)C.[CH3:34][O:35][CH2:36][CH2:37][O:38][CH2:39]Cl>C(Cl)Cl>[CH3:22][O:21][C:9]1[C:8]([CH3:23])=[C:7]2[C:3]([C:4](=[O:24])[O:5][CH2:6]2)=[C:2]([O:1][CH2:34][O:35][CH2:36][CH2:37][O:38][CH3:39])[C:10]=1[CH2:11]/[CH:12]=[C:13](\[CH3:20])/[CH2:14][CH2:15][C:16]([O:18][CH3:19])=[O:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To methyl (E) 6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate (61.0 g) in methylene chloride (1000 ml) at 0° C. was added diisopropylethylamine (30.4 g) and methoxyethoxymethyl chloride (29.2 g). After 31/2 hours the solution was washed with dilute hydrochloric acid, dried and evaporated to give methyl (E) 6-(1,3-dihydro-6-methoxy-4-methoxyethoxymethoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate as an oil.
Workup
- washAfter 31/2 hours the solution was washed with dilute hydrochloric acid
- customdried
- customevaporated
Sources & evidence
- ORD record
- ord-4d71fc8be3b04f5ba24d61ccff0b930e
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05493030
Reaction notes
Loading…