HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 11953279, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 11953280 | HCID 11953280 | — |
| Product | HCID 11953279 | HCID 11953279 | 78.9% |
Reaction Steps
1,5-Bis(4-amino-3-hydroxyphenoxy)naphthalene was synthesized in a manner analogous to Example 2 from 1,5-bis(3-hydroxy-4-nitrophenoxy)naphthalene. Yield: 78.9%; mp 251˜253° C., IR (KBr) 3292, 3365, 1498 cm−1; MS (EI) m/z 374 (M+, 100); Elemental Anal. Calcd. for C22H18N2O4: C, 70.59; H, 4.81; N, 7.49. Found: C, 70.48; H, 4.88; N, 7.46.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365231B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-36c96b595e5641278d1c798312faa852 |
| Source note | uspto-grants-2008_04 |