HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → N-(2,2-Dimethoxyethyl)prop-2-yn-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(2,2-Dimethoxyethyl)prop-2-yn-1-amine | HCID 20307436 | — |
Reaction Steps
N-(2,2-Dimethoxyethyl)amine (23 grams), triethylamine (31 ml) and benzene (100 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. 1-Bromo-2-propyne (16.5 grams) was added dropwise with stirring to the reaction mixture at room temperature. After the addition was completed stirring was continued for a period of about 1 hour. After this time the reaction mixture was filtered and stripped of solvent. The residue was then distilled to yield the desired product N-propargyl-N-(2,2-dimethoxyethyl)amine having a boiling point of 70° C. at 1 mm of Hg pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04113464 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-aa97379b6455429a9aaa962c31176061 |
| Source note | uspto-grants-1978_09 |