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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886893Generated: October 26, 2026

1-Methylimidazole → 4-(1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-yloxy)-4-oxobutanoic acid triethylamine salt

https://huagongshe.com/reaction/1886893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantSuccinic anhydrideHCID 7922—
ReactantTriethylamineHCID 8471—
Reactant1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-olHCID 68748764—
SolventDichloromethaneHCID 6344—
Product4-(1-(Bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-yloxy)-4-oxobutanoic acid triethylamine saltHCID 68746889—

Reaction Steps

1-(bis(4-methoxyphenyl)(phenyl)methoxy)icosan-3-ol (6.8 g, 11.0 mmoles), succinic anhydride (1.1 g, 11.0 mmoles), triethylamine (4.6 mL, 33.0 mmoles) and 1-methylimidazole (0.44 mL, 5.5 mmoles) are dissolved in methylene chloride (68 mL). The reaction is stirred at ambient temperature for five days, during which time the solution darkened. The solution is then diluted with methylene chloride (100 mL) and washed twice with ice-cold aqueous citric acid (10% [w/v], 50 mL) and once with saturated aqueous sodium chloride (50 mL). The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and evaporated to a dark resin. The crude product is purified on silica gel (200 mL bed volume) eluting with methylene chloride:triethylamine (95:5 [v/v/v], 500 mL), then methylene chloride:methanol:triethylamine (93:2:5 [v/v/v], 1000 mL). Fractions containing pure product by thin layer chromatography are pooled and evaporated to a resin. The resin is dried well in vacuo. The yield is 2.4 g (30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501706B2
Source datasetuspto-grants-2013_08
ORD IDord-ddd8ad3cc9354c3692719c4d2c851518
Source noteuspto-grants-2013_08