HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 2-Phenoxyphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Isobutylamine Hydrochloride | HCID 12206183 | — |
| Product | 2-Phenoxyphenylacetonitrile | HCID 141221 | — |
Reaction Steps
3-Phenoxybenzaldehyde, isobutylamine hydrochloride and sodium cyanide were reacted on a 0.3 molar scale using essentially the same procedure as that described in Example 1. The product, α-(N-isobutylamino)-3-(phenoxybenzeneacetonitrile, was obtained as a golden oil (43.5 g). Proton nuclear magnetic resonance spectrum (d6 -acetone; δ in ppm): 0.9 (6H, d of d); 1.74 (1H, m); 2.52 (2H, d); 5.02 (1H, s); 6.9-7.6 (9H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420614 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-da0132e4c21d443f8daf4f8b4a106b6a |
| Source note | uspto-grants-1983_12 |