HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2-(2,3-Dihydrobenzofuran-5-yl)-1-morpholinoethanethione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1-(2,3-Dihydro-5-benzofuranyl)ethanone | HCID 145220 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2,3-Dihydrobenzofuran-5-yl)-1-morpholinoethanethione | HCID 13704380 | — |
Reaction Steps
Morpholine (1.5 ml), 2,3-dihydro-5-acetylbenzofuran (2.0 g), sulfur (0.395 g) and p-toluene sulfonic acid (0.060 g) were heated at reflux. After 3 hours, the reaction mixture was cooled and 6 ml of methanol added. This solution was further cooled which precipitated the morpholide. The precipitate was filtered and washed with cold methanol to give 2,3-dihydrobenzofuran-5-ylthioacetic acid morpholide, m.p.--144°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04780480 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-9d3301cc607748479d10fed339056f31 |
| Source note | uspto-grants-1988_10 |