HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 20285729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphine, triphenyl-, hydrobromide | HCID 517696 | — |
| Reactant | HCID 20285713 | HCID 20285713 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | HCID 20285729 | HCID 20285729 | — |
Reaction Steps
14.0 G. of 2,4-dimethyl-3-hydroxymethyl-5-(methylthio)thiophene and 26.0 G. of triphenylphosphonium bromide were dissolved in 75 ml. of acetonitrile and stirred at 40° C. for 1 hour. The resulting mixture was cooled and poured into 150 ml. of ethyl acetate then treated with ethyl ether/hexane (5:1). The resulting solution was decanted from a gum-like residue. The residue was treated with hot acetone and the resulting white crystals were filtered, washed with cold acetone and dried under high vacuum at 80° C. to yield [2,4-dimethyl-5-(methylthio)-3-thenyl]triphenylphosphonium bromide, m.p. 245°-248° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04230872 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-50ab04fcd61747a1b3ddd7d0fdf16e8a |
| Source note | uspto-grants-1980_10 |