HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 53679807, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14997927 | HCID 14997927 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53679807 | HCID 53679807 | — |
Reaction Steps
70.2 Grams of 4-[(2-ethylhexyl)oxy]benzaldehyde (prepared as described in the preceding paragraph) and 38.6 g of phenylacetonitrile were added to 800 ml of methanol and stirred cold (10°-15° C.). To this was added (dropwise) 125 ml of aqueous sodium hydroxide (50 percent) with continued stirring at 10°-15° C. for an additional two hours. The mixture was then stirred overnight at room temperature and then poured into cold water and extracted with ethyl acetate. The extract was dried and evaporated to yield α-[[4-(2-ethylhexyloxy)phenyl]methylene]benzeneacetonitrile which was catalytically reduced as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05135955 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-d38db798624445e389840e62b89e7a93 |
| Source note | uspto-grants-1992_08 |