HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-hydroxy-N-(3-benzo[b]thien-2-ylprop-2-enyl) acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydropyranyl hydroxylamine | HCID 13168123 | — |
| Reactant | 3-Benzo[b]thienylbromoprop-2-ene | HCID 19846335 | — |
| Reactant | O-Tetrahydropyranyl-3-benzo[b]thien-2-ylprop-2-enyl hydroxylamine | HCID 86743434 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-hydroxy-N-(3-benzo[b]thien-2-ylprop-2-enyl) acetamide | HCID 24103629 | 66% |
Reaction Steps
O-Tetrahydropyranyl-3-benzo[b]thien-2-ylprop-2-enyl hydroxylamine. Tetrahydropyranylhydroxyl amine (0.51 g, 4.34 mmole) in DMF (10 mL) was added to a solution of 3-benzo[b]thienylbromoprop-2-ene (0.50 g, 1.98 mmole) in DMF (10 mL). After being allowed to stir for two hours the reaction was poured into water and extracted with ether. The organic layer was washed with NaHCO3 and brine. The organic layer was dried over MgSO4 and evaporated. The residue was chromatographed on silica gel eluting with 40% ether in hexanes to give the desired product as a yellow oil (66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04873259 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-18a37d57f339492d9e98a2d2ddc0525b |
| Source note | uspto-grants-1989_10 |