HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 11953165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 11953164 | HCID 11953164 | — |
| Product | HCID 11953165 | HCID 11953165 | 81% |
Reaction Steps
1,3-Bis(4-amino-3-hydroxyphenoxy)benzene was synthesized in a manner analogous to Example 2 from 1,3-bis(3-hydroxy-4-nitrophenoxy)benzene. Yield: 81%; mp 171˜174° C.; IR (KBr): 3414, 3342, 1588, 1518 cm−1; MS (EI) m/z 324 (M+, 100); Elemental Anal. Calcd. for C18H16N2O4: C, 66.67; H, 4.94; N, 8.64. Found: C, 66.45; H, 5.02; N, 8.53.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365231B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-b9fa64e8c7c6447983d142f6362ee3bd |
| Source note | uspto-grants-2008_04 |