HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217317Generated: October 30, 2026
Dimethyl Sulfoxide → p-(6-Methoxy-2-phenyl-3,4-dihydro-1-naphthyl)phenol
https://huagongshe.com/reaction/217317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-Iodo-7-methoxy-3-phenyl-4-(4-pivaloyloxyphenyl)-1,2,3,4-tetrahydronaphthalene | HCID 25111989 | — |
| Product | p-(6-Methoxy-2-phenyl-3,4-dihydro-1-naphthyl)phenol | HCID 200362 | 89% |
Reaction Steps
Potassium tert-butoxide solution 0.5 mol/L in dimethyl sulfoxide (1.10 mL, 0.55 mmol) was added to and dissolved in 2-iodo-7-methoxy-3-phenyl-4-(4-pivaloyloxyphenyl)-1,2,3,4-tetrahydronaphthalene (5′, 74.4 mg, 0.138 mmol) under an argon atmosphere, and the resulting aubergine solution was stirred for 1 hour while heating at 90° C. Thereafter, the reaction mixture was cooled with ice, and then a saturated aqueous ammonium chloride solution (7 mL) was added thereto and sufficiently stirred, followed by extracting four times with a mixed liquid (4 mL) of hexane/diethyl ether (1:1). An organic layer was collected, followed by drying with anhydrous magnesium sulfate and concentration thereof. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) to obtain the title compound (7, 41.1 mg, yield 89%), the same as that of Example 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193394B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-19e120eb913043daac4897823a87ca2f |
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| Source note | uspto-grants-2012_06 |
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