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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380008Generated: November 2, 2026

HCID 18956456, compound → HCID 18956464, compound

https://huagongshe.com/reaction/2380008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18956456HCID 18956456—
CatalystZincHCID 23994—
SolventAcetonitrileHCID 6342—
ProductHCID 18956464HCID 1895646483.4%

Reaction Steps

The product of the previous preparation, 3-(2-Bromotetrafluoroethoxy)-N-(4-(2-bromotetrafluoroethoxy)phenyl) phthalimide, (2.73 g, 0.00445 mole) is dissolved in 20 ml of warm acetonitrile (approximately 50° C.) and added to zinc metal (0.61 g, 0.0093 mole) in 5 ml of acetonitrile stirring at reflux. The reaction mixture is stirred at reflux for 12 hours, then filtered on a fine-pored fritted glass funnel to remove unreacted zinc and zinc halide salts. The precipitate is washed twice with 25 ml of dichloromethane, and the filtrates are combined with the acetonitrile flitrate and evaporated to dryness. The dry residue is dissolved in 15 ml of dichloromethane/hexane (1:1, v/v (volume/volume)) and subjected to column chromatography on neutral alumina using dichloromethane/hexane (1:4, v/v) to provide the product (1.54 g, 83.4 percent yield) as a light yellow solid with a melting point of 160°-160.5° C. IR (cm-1): 1721, 1708, 1322, 1121 (imide), 1289, 1282, 1273, 1213, 1191, 1166, 1146, 1110, 1096 (C-O, C-F), 1514, 808, 801,743 (aromatic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364917
Source datasetuspto-grants-1994_11
ORD IDord-dd0d718c15434e9dbecf6873d223fc05
Source noteuspto-grants-1994_11