Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (8-(Benzyloxymethyl)-1,4-dioxaspiro[4.5]decan-8-yl)methanol | HCID 58399365 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 58399448 | HCID 58399448 | 95% |
Reaction Steps
To a solution of (8-(benzyloxymethyl)-1,4-dioxaspiro[4.5]decan-8-yl)methanol (Reference Example 85) (183 mg, 0.625 mmol) in dimethyl sulfoxide (2.1 mL), 50% sulfur trioxide-pyridine complex (596 mg, 1.87 mmol) and triethylamine (0.522 mL, 3.75 mmol) were added, and the obtained solution was stirred at room temperature for 20 minutes. The reaction was quenched by adding water to the reaction solution, and the resulting solution was extracted with ethyl acetate. The organic layer was washed sequentially with 20% aqueous citric acid solution, saturated sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (172 mg, 0.592 mmol, 95%) as a colorless oily compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247569B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-20f01417b2834234bd8c7c0d7877a088 |
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| Source note | uspto-grants-2012_08 |
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