Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 54071153 | HCID 54071153 | — |
| Reactant | HCID 54157760 | HCID 54157760 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54097591 | HCID 54097591 | 41.8% |
Reaction Steps
0.2 g of N,N'-dicyclodicyclohexylcarbodiimide was added at room temperature while stirring to a solution of 0.6 g of 2,5-bis(4-[6-acryloyloxyhexyloxy]phenylcarboxy)benzoic acid, 0.4 g of 4-[4-(2-amino-5-nitro-4-[(S)-2-octyloxy]-phenyl)benzoyloxy]phenylmethanol and 0.04 g of 4-dimethylaminopyridine in 20 ml of dichloromethane. The reaction mixture was stirred at room temperature overnight, poured into 100 ml of water and then extracted three times with 50 ml of dichloromethane each time. The organic phases were washed twice with 100 ml of water each time, dried over magnesium sulphate, filtered and subsequently concentrated. Chromatographic purification of the residue on silica gel with hexane/ethyl acetate (vol. 1:1) and two-fold recrystallization from acetone of the fractions which were pure according to thin-layer chromatography gave 0.4 g of (4-[4-(2-amino-5-nitro-4-[(S)-2-octyloxy]phenyl)benzoyloxy]phenyl)-methyl 2,5-bis(4-[6-acryloyloxyhexyloxy]phenylcarboxy)benzoate; m.p. (C-I) 100° C., Sc* -N*, 96° C., cl.p. (N* -I) 100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650534 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-457e1000cc584aa593fcd32943613de0 |
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| Source note | uspto-grants-1997_07 |
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