Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Tiglic acid | HCID 125468 | — |
| Reactant | HCID 59439471 | HCID 59439471 | — |
| Solvent | Methanesulfonic Acid | HCID 6395 | — |
| Product | HCID 59439459 | HCID 59439459 | — |
Reaction Steps
A solution of 5.79 g (27.5 mmol) of 2-(2-hydroxy-6-methoxyphenyl)ethyl acetate, 3.03 g (30.3 mmol) of 2-methylcrotonic acid and 3.26 g (16.9 mmol) of diphosphorus pentaoxide in 29.0 mL of methanesulfonic acid was heated and stirred at 70° C. for 75 minutes. 50 mL of toluene and 50 mL of water were added therein at room temperature and the mixture was stirred for 5 minutes, and then transferred to a separatory funnel and settled. The aqueous layer was separated and discarded and after the organic layer was washed with 25 mL of 5% sodium hydrogen carbonate aqueous solution and 25 mL of water sequentially, the solvent was evaporated to obtain 7.85 g of the crude title compound. This was purified by silica gel chromatography (developing solution composition: 10% ethyl acetate-hexane (volume ratio), Rf: 0.4), and 2.96 g of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110688B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-7fddb4bc3c924c48adf9a469a56c34a9 |
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| Source note | uspto-grants-2012_02 |
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