HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3,4-Dimethylphenyl)acetonitrile → 2-(3,4-dimethylphenyl)-N'-hydroxyethanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3,4-Dimethylphenyl)acetonitrile | HCID 76401 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3,4-dimethylphenyl)-N'-hydroxyethanimidamide | HCID 5187867 | 93% |
Reaction Steps
3,4-Dimethylphenylacetonitrile (10 g, 0.069 mol) was added to a mixture of hydroxylamine hydrochloride (9.57 g, 0.14 mol), methanol (100 mL) and 25% sodium methoxide/methanol (31.5 mL, 0.14 mol) at room temperature. After stirring for 16 hours at room temperature, the reaction mixture was concentrated in vacuo. The resultant oil was partitioned between methylene chloride and water. The organic phase was separated, washed with water, dried over magnesium sulfate and concentrated in vacuo to yield the desired product (11.4 g, 93%) as a white solid. Recrystallization from toluene afforded an analytical sample m.p. 59°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04895862 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-2151eb6996b04815873593e7d1dea55c |
| Source note | uspto-grants-1990_01 |