HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-chloro-5-nitrocinnamic acid-N-methyl-N-hexylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-Methylhexylamine | HCID 37079 | — |
| Reactant | HCID 54271341 | HCID 54271341 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-chloro-5-nitrocinnamic acid-N-methyl-N-hexylamide | HCID 53721375 | 81% |
Reaction Steps
At 0° to 5° C., 11.5 g (0.10 mol) of N-methylhexylamine in 100 ml of tetrahydrofuran was added to a solution of 12.3 g (0.05 mol) of 2-chloro5-nitrocinnamyl chloride in 40 ml of tetrahydrofuran. After the mixture had been stirred for 2 hours, the solvent was removed, and the residue thus obtained was dissolved in ethyl acetate and extracted with 5% strength sodium hydroxide solution. The organic phase was washed with water, followed by separation and drying, to give 13.3 g (81% of theory) of 2-chloro-5-nitrocinnamic acid-N-methyl-N-hexylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05009701 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-6e5bbcb0cb1941e198c399ff15951cc1 |
| Source note | uspto-grants-1991_04 |