HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 7-Oxo-5-octenoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | Methyl 2-formylbutanoate | HCID 15570303 | — |
| Product | 7-Oxo-5-octenoic acid methyl ester | HCID 57059549 | — |
Reaction Steps
Methyl formylbutyrate (13 g) and 1-triphenylphosphoranylidene-2-propanone (31.4 g) were refluxed together in toluene (200 ml) for 30 minutes. The toluene was then evaporated off and ether (200 ml) added to the residue to give a suspension which was stirred at room temperature for 5 minutes. The suspended triphenylphosphine oxide was filtered off and washed with a further 100 ml of ether. The combined ether solutions were evaporated to dryness to give a yellow oil which was distilled at 0.1 mm Hg using a Kugelrohr apparatus (air bath temperature 140° C.) to yield 7-oxo-5-octenoic acid methyl ester as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04513005 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-ce739595dd96443b94ad8c7fab665b16 |
| Source note | uspto-grants-1985_04 |