HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-formylphenyl)acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-dimethoxymethylphenyl)acrylamide | HCID 68819697 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (E)-N-(4'-chlorobiphenyl-4-yl)-3-(4-formylphenyl)acrylamide | HCID 86601892 | — |
Reaction Steps
70 mL of water and 21 mL of trifluoroacetic acid are added to a suspension of 9.8 g (24.02 mmol) of (E)-N-(4′-chlorobiphenyl-4-yl)-3-(4-dimethoxymethylphenyl)acrylamide in 280 mL of chloroform and the reaction mixture is stirred for 8 hours at ambient temperature. It is diluted with chloroform and water, the organic phase is separated off and extracted with water. The organic phase is dried, filtered through silica gel, and the solvent is distilled off. Yield: 5.5 g; C22H16ClNO2 (M=361.83); calc.: molecular ion peak (M+H)+: 362/364; found: molecular ion peak (M+H)+: 362/364; Rf value: 0.6 (silica gel, cyclohexane/ethyl acetate (1:1)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592373B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-f3f23132980c40bbb6fe53683a7d8269 |
| Source note | uspto-grants-2009_09 |