Water → HCID 23043525, compound
Reaction equation
[H-].[Na+].[CH2:3](Br)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.COC1C=CC(C(C2C=CC=CC=2)(C2C=CC=CC=2)[O:20][CH2:21][CH:22]([OH:41])[CH2:23][O:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][O:33][CH2:34][CH2:35][O:36][CH2:37][CH2:38][O:39][CH3:40])=CC=1.O>CN(C)C=O>[C:4]1([CH2:3][O:41][CH:22]([CH2:21][OH:20])[CH2:23][O:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][O:33][CH2:34][CH2:35][O:36][CH2:37][CH2:38][O:39][CH3:40])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred suspension of 3.26 g of unwashed 50% sodium hydride and 10.9 g of benzyl bromide in 40 ml of dimethylformamide, under argon, was added a solution of 27.14 g of 20-[(4-methoxyphenyl)diphenylmethoxy]-2,5,8,17-tetraoxaeicosan-19-ol in 50 ml of dimethylformamide over 1/2hour. This mixture was stirred overnight, water was then added and the mixture extracted with ether. The ether extract was washed with water, dried and the solvent removed. The residue was dissolved in hot methanol and stirred with 10 g of a strongly acidic ion exchange resin. This mixture was filtered and the solvent removed. The residue was purified by HPLC, eluting with hexane:ethyl acetate (65:35) giving the desired compound as 12.9 g of a light yellow oil.
Workup
- extractionthe mixture extracted with ether
- extractionThe ether extract
- washwas washed with water
- customdried
- customthe solvent removed
- dissolutionThe residue was dissolved in hot methanol
- stirringstirred with 10 g of a strongly acidic ion exchange resin
- filtrationThis mixture was filtered
- customthe solvent removed
- customThe residue was purified by HPLC
- washeluting with hexane:ethyl acetate (65:35)
Sources & evidence
- ORD record
- ord-28d26d424b5e4966bb45cee1d679f730
- Source dataset
- uspto-grants-1987_10
- Patent number
- US04703130
Reaction notes
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