HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511711Generated: November 1, 2026
6-[((2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)prop-2-enoyl)oxy]hexyl 3,5-dinitrobenzoate → 6-[((2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)-phenyl]-methoxy}-phenyl)-prop-2-enoyl)oxy]hexyl 3,5-diaminobenzoate
https://huagongshe.com/reaction/511711
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-[((2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)prop-2-enoyl)oxy]hexyl 3,5-dinitrobenzoate | HCID 86676547 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-[((2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)-phenyl]-methoxy}-phenyl)-prop-2-enoyl)oxy]hexyl 3,5-diaminobenzoate | HCID 86676548 | 83.1% |
Reaction Steps
5.95 g (8.38 mmol) of 6-[((2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)-prop-2-enoyl)oxy]-hexyl 3,5-dinitrobenzoate are dissolved in a mixture of 54 mL of N,N-di-methylformamide and 6 mL water. 13.9 g (51.4 mmol) ferric chloride hexahydrate is added. 5.60 g (85.7 mmol) zinc powder is added portion wise within 60 minutes. The mixture is allowed to react for 2 hours. The reaction mixture is partitioned between ethyl acetate and water and filtrated. The organic phase is washed repeatedly with water, dried over sodium sulfate, filtrated and concentrated under reduced pressure. Filtration of the residue on 200 g silica gel using toluene:ethyl acetate 1:3 as eluent and crystallization from ethyl acetate:hexane mixture yields 4.53 g of 6-[((2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)-phenyl]-methoxy}-phenyl)-prop-2-enoyl)oxy]hexyl 3,5-diaminobenzoate as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09097938B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-376d7ca2fef6429aa5834797aa012eda |
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| Source note | uspto-grants-2015_08 |
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