Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-((6-(Acryloyloxy)hexyl)oxy)benzoic acid | HCID 3713565 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 21072080 | HCID 21072080 | — |
Reaction Steps
A reaction flask was charged with 11.08 g (0.038 moles) of 4-{[6-(acryloyloxy)hexyl]oxy}benzoic acid, 7.67 g (0.076 moles) of triethylamine and 110 g of ethylene glycol dimethyl ether. The solution was cooled to −30° C., and 4.34 g (0.038 moles) of methane sulfonyl chloride was added. After maintaining stirring at −30° C. for one additional hour, 9.09 g (0.038 moles) of intermediate 6 and 0.46 g (0.004 moles) of 4-(dimethylamino)pyridine were added. The resulting mixture was then warmed to room temperature, and then to 50° C. for three hours. Finally, the mixture was cooled to room temperature and diluted with 300 ml of water. The crude product was collected by filtration and washed with water. The product, 7, was purified by recrystallization from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160586B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-bdf0e0d0258241deb9cd575789f0570b |
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| Source note | uspto-grants-2007_01 |
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