HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722840Generated: November 1, 2026
Isopropenyl acetate → HCID 57308969, compound
https://huagongshe.com/reaction/1722840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | HCID 20027798 | HCID 20027798 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57308969 | HCID 57308969 | — |
Reaction Steps
A mixture of 4-(3-bromopropyloxy)-γ-oxo-β-methylbenzenebutanoic acid (50 g), anhydrous cupric sulfate (50 g), isopropenyl acetate (200 ml) and toluene (200 ml) was refluxed in an atmosphere of nitrogen for 30 minutes during which about 150 ml of the distillate was collected. The mixture was cooled, diluted with ethyl acetate (150 ml) and filtered through a bed of Celite. The solid was washed with ethyl acetate (150 ml) and the combined filtrates were washed with saturated NaHCO3 (100 ml×4), brine (100 ml×2) and dried over Na2SO4. The organic layer was concentrated and the residue was dissolved in ethyl acetate (about 300 ml). Platinum oxide (PtO2) (3.0 g) was added and the cooled (about 10° C.) mixture was hydrogenated at 20 p.s.i. H2 pressure for 90 minutes. The mixture was filtered, concentrated and the residue was purified by (suction) chromatography on silica gel to provide the title compound as an oil, uncontaminated with the (5S, 4S) and (5R, 4R) diastereomers as determined by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857659 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-50edc7545ca64bebbbf362d3a30c9e05 |
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| Source note | uspto-grants-1989_08 |
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