Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium metaborate | HCID 145326 | — |
| Reactant | Aminoammonium hydroxide | HCID 44558531 | — |
| Reactant | HCID 57552323 | HCID 57552323 | — |
| Reactant | HCID 57552327 | HCID 57552327 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57552324 | HCID 57552324 | — |
Reaction Steps
18.2 g (56.6 mmol) of methyl 5-propyl-2-trifluoromethanesulfonyloxycyclohex-1-enecarboxylate, 21.5 g (74.6 mmol) of 4-ethoxy-3-fluoro-2-(2-methoxyethoxymethoxy)benzeneboronic acid, 1.5 ml of water, 33 g (120 mmol) of sodium metaborate, 1.12 g (1.6 mmol) of bis(triphenylphosphine)palladium(II) chloride and 0.1 ml (1.6 mmol) of hydrazinium hydroxide are heated under reflux overnight in 300 ml of tetrahydrofuran. After addition of water, the aqueous phase is separated off and extracted twice with MTB ether. The combined organic phases are washed with saturated sodium chloride soln. and dried over sodium sulfate. The solvent is removed under reduced pressure, and the residue is filtered through silica gel with n-heptane/MTB ether (6:4), giving 3-ethoxy-4-fluoro-8-propyl-7,8,9,10-tetrahydrobenzo[c]chromen-6-one as colourless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07824745B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-4a0d819ddab24527bb2cfaab3e96d396 |
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| Source note | uspto-grants-2010_11 |
|---|