HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylamide → 3-[{2-(1,3-Benzodioxol-5-yl)ethyl}thio]propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | 2-(1,3-Benzodioxol-5-yl)ethanethiol | HCID 15819512 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[{2-(1,3-Benzodioxol-5-yl)ethyl}thio]propionamide | HCID 19001682 | 60.4% |
Reaction Steps
5 g of 2-(1,3-benzodioxol-5-yl)ethanethiol and 4 g of acrylamide were dissolved in 100 ml of ethanol and the solution was heated under reflux to conduct the reaction for 20 h. The reaction mixture was cooled with ice. 100 ml of ethanol was added thereto and crystals thus formed were recovered by filtration to obtain 4.2 g of the intended compound in the form of colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05475024 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-47aaf99627ea4e2093946d2b4eb65c62 |
| Source note | uspto-grants-1995_12 |