HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → Benzenamine, N-2-propyn-1-yl-4-(trifluoromethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(Trifluoromethoxy)aniline | HCID 600848 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane heptane | HCID 21907733 | — |
| Product | Benzenamine, N-2-propyn-1-yl-4-(trifluoromethoxy)- | HCID 14650037 | 66.2% |
Reaction Steps
A solution of 8.86 g (50 mmol) of 4-(trifluoromethoxy)benzenamine, 8.18 g (55 mmol) of an 80% solution of 3-bromo-1-propyne in toluene, and 8.72 ml (50 mmol) of N-ethyl-N-(1-methylethyl)-2-propanamine in 200 ml of toluene is heated at 90° C. for eighteen hours. The suspension is cooled and treated with ethyl acetate. The suspension is washed several times with water. The ethyl acetate layer is separated, dried (magnesium sulfate), and concentrated to give a brown liquid. This is applied to a column of 1 kg of flash silica gel packed in n-heptane-dichloromethane (2:1). Elution with the same solvent gives 7.12 g (66.2%) of the product as a brown liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857530 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-97384ccf920e42868cb46dba25b9d8f7 |
| Source note | uspto-grants-1989_08 |