HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → Benzeneacetonitrile, alpha-ethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Product | Benzeneacetonitrile, alpha-ethyl- | HCID 95334 | 98% |
Reaction Steps
Using the method of Procedure A.(a) 1, alkylation of phenylacetonitrile with ethyl bromide gave a 98% yield of the title compound, b.p. 110°-116° at 13 mm. (Lit.1 b.p. 124°-126° at 25 mm.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04127720 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-e8130fd59e484bacb167a7455fc22235 |
| Source note | uspto-grants-1978_11 |