HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 102287610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 118513273 | HCID 118513273 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 102287610 | HCID 102287610 | — |
Reaction Steps
To a solution of 2-allyl-4-(trifluoromethoxy)aniline (17.5 g, 80.6 mmol) in THF (1000 ml), cooled in a dry ice bath to a temperature below −10° C. was added Et3N (8.96 g, 17.3 mmol) and acryloyl chloride (7.98 g, 88.7 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 1 hr. The resulting mixture was concentrated under reduced pressure, dissolved in ethyl acetate, washed with water and brine. The organic portion was dried over Na2SO4, filtered and concentrated in under reduced pressure to give a white solid which was washed with ethyl acetate to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403833B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-e283f2b96d4f44fab1f529f8633d90c9 |
| Source note | uspto-grants-2016_08 |