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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511731Generated: November 1, 2026

HCID 86676571, compound → HCID 86676570, compound

https://huagongshe.com/reaction/511731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86676571HCID 86676571—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86676570HCID 8667657087.4%

Reaction Steps

9.57 g (8.38 mmol) of 2,2-bis(4-nitrobenzyl)-3-{[(2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoyl]oxy}propyl (2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoate are dissolved in a mixture of 54 mL of N,N-dimethylformamide and 6 mL water. 13.9 g (51.4 mmol) ferric chloride hexahydrate are 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 400 g silica gel using toluene:ethyl acetate 1:3 as eluent and crystallization from ethyl acetate:hexane mixture yields 7.93 g of 2,2-bis(4-aminobenzyl)-3-{[(2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoyl]oxy}propyl (2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoate as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09097938B2
Source datasetuspto-grants-2015_08
ORD IDord-79401334f9cc4b329414e494ab037a34
Source noteuspto-grants-2015_08