HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(2,5-Dimethoxyphenyl)-2-methyl-4-phenyl-1-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzyl acetone | HCID 17355 | — |
| Reactant | (2,5-Dimethoxybenzyl)(triphenyl)phosphonium bromide | HCID 19605777 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2,5-Dimethoxyphenyl)-2-methyl-4-phenyl-1-butene | HCID 53893518 | — |
Reaction Steps
A solution of n-butyl lithium (29 ml. of 2.2 M) is added dropwise to 2,5-dimethoxybenzyl triphenylphosphonium bromide (31.5 g.) in tetrahydrofuran (200 ml.) with stirring and the resulting deep red solution is stirred for one-half hour. Benzyl acetone (9.4 g.) is added dropwise and the reaction mixture stirred for 12 hours. It is then adjusted to pH 7 by addition of acetic acid and concentrated under reduced pressure. The residue is extracted with methylene chloride and the extract evaporated to give crude 1-(2,5-dimethoxyphenyl)-2-methyl-4-phenyl-1-butene as an oil. It is purified by chromatography on silica gel and elution with benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04206225 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-14ce2b34e5d0457f9fb24ff54c68fd53 |
| Source note | uspto-grants-1980_06 |