Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 85999797 | HCID 85999797 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 10096933 | HCID 10096933 | — |
Reaction Steps
A mixture of 2,6-bis(3-chloropropyloxy)naphthalene(1 gm, 0.003 mole) and p-anisidine(1.17 gm, 0.005 mole) was taken in 60 ml dry DMSO. It was refluxed at 140° C. for 12 hrs. The completion of the reaction was checked by TLC. The reaction mixture was poured into distilled water (80 ml) and extracted with ethyl acetate thrice. The organic layer was separated and concentrated to get oily compound which was further crystallized by benzene hexane to get the desired compound, m.p. 129° C., (yield 1.4 gm, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081465B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-8602afcfcfc34702adeae4b8cb6b6cad |
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| Source note | uspto-grants-2006_07 |
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