HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4,4-Diphenyl-5-hydroxyl-6-heptenenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4,4-Diphenyl-4-formylbutanenitrile | HCID 19610274 | — |
| Reactant | HCID 178420667 | HCID 178420667 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-Diphenyl-5-hydroxyl-6-heptenenitrile | HCID 19045741 | — |
Reaction Steps
Under argon gas, 4,4-diphenyl-4-formylbutanenitrile (5.0 g) was dissolved in dry tetrahydrofuran (200 ml). Then, 1M vinylmagnesium bromide-tetrahydrofuran (30 ml) was added dropwise -40° C. After completion of addition, the reaction temperature was allowed to rise gradually to 0° C. (over 3 hours). After completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction mixture and the insoluble matter was filtered off. The filtrate was extracted with ethyl acetate, washed, dried, and concentrated and the group was purified by silica gel column chromatography. The active fraction was concentrated to provide the title compound as oil (5.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633248 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-206c74739b404c849cda9be7a167a4f0 |
| Source note | uspto-grants-1997_05 |