Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 22022382 | HCID 22022382 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 11755168 | HCID 11755168 | — |
Reaction Steps
A mixture of 2,7-bis(3-chloropropyloxy)naphthalene (1 gm, 0.003 mole) and p-anisidine (1.17 gm, 0.005 mole) were 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 as solid, m.p. 127° C., (yield 1.34 gm, 89%).
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-20916a283f7b4e35ae8b97c1acc5e84b |
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| Source note | uspto-grants-2006_07 |
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