HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433924Generated: October 27, 2026
Water → Naphthalene, 1,2-dihydro-3-(4-methoxy-2-nitrophenyl)-7-(phenylmethoxy)-
https://huagongshe.com/reaction/1433924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Bromo-3-nitroanisole | HCID 79288 | — |
| Reactant | 3-Bromo-1,2-dihydro-7-(phenylmethoxy)naphthalene | HCID 23087420 | — |
| Catalyst | Copper | HCID 23978 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Naphthalene, 1,2-dihydro-3-(4-methoxy-2-nitrophenyl)-7-(phenylmethoxy)- | HCID 23087493 | 40.7% |
Reaction Steps
The title compound was synthesized by referring to Tetrahedron Lett., 1993, 34 (21), 3421. A suspension of 7-benzyloxy-3-bromo-1,2-dihydronaphthalene (38 g), 4-bromo-3-nitroanisole (59 g), dichlorobis(triphenylphosphine)palladium (II) (4.5 g) and copper (32 g) in dimethyl sulfoxide (400 ml) was stirred under a nitrogen atmosphere at 120° C. for 1 hour. Ethyl acetate and water was added thereto, the solution was filtered through celite pad, extracted with ethyl acetate, then sequentially washed with aqueous ammonia, water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612114B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-fda9d973ee9f4a98b5d11358fc070fac |
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| Source note | uspto-grants-2009_11 |
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