Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylamine | HCID 8085 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 68691874 | HCID 68691874 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68698119 | HCID 68698119 | — |
Reaction Steps
To a solution of the phenol product obtained from step 6 of Example 3 (0.38 g, 1.0 mmol) and diisobutylamine (18 μL, 0.10 mmol) in toluene (5 mL) was added dropwise sulfuryl chloride (80 μL, 1.0 mmol) over 10 min. The resulting solution was stirred at 25° C. for 1 h and then quenched with a saturated solution of aqueous sodium bicarbonate. The organic layer was extracted with ethyl acetate and the combined organic layer was washed with 2 N solution of sodium sulfite. After removal of the solvent, the crude product was purified by chromatography on silica gel eluting with 7:3 hexane:ethyl acetate to give the title product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834036B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-aa567c8373764acb86a6f72e5619b3f8 |
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| Source note | uspto-grants-2010_11 |
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