HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380008Generated: November 2, 2026
HCID 18956456, compound → HCID 18956464, compound
https://huagongshe.com/reaction/2380008
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 18956456 | HCID 18956456 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18956464 | HCID 18956464 | 83.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05364917 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-dd0d718c15434e9dbecf6873d223fc05 |
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| Source note | uspto-grants-1994_11 |
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