HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzenamine, 4-ethenyl-N,N-diphenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | — |
| Product | Benzenamine, 4-ethenyl-N,N-diphenyl- | HCID 10869403 | 89% |
Reaction Steps
Thereafter, 20 g (0.066 mol) of 4-(diphenylamino)benzaldehyde (1) dissolved in 40 ml of THF was charged into the dropping funnel, and was gradually added dropwise to the mixture. After the addition, a reaction was caused at room temperature for 2 hours. Then, 70 ml of water was added thereto. The product was extracted with ethyl acetate, and the extract was washed with water until neutralized. The organic phase was dried, concentrated and then purified by column chromatography. Pale yellow crystals of 4-(diphenylamino)styrene (3) (16 g, yield: 89%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09304417B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-0f4f1bd1023441afa1fafed63d9b72a5 |
| Source note | uspto-grants-2016_04 |