HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 11953168, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 11953218 | HCID 11953218 | — |
| Product | HCID 11953168 | HCID 11953168 | 80.2% |
Reaction Steps
1,4-Bis(4-amino-3-hydroxyphenoxy)-2-tert-butyl benzene was synthesized in a manner analogous to Example 2 from 1,4-bis(3-hydroxy-4-nitrophenoxy)-2-tert-butyl benzene. Yield: 80.2%; mp 110˜113° C.; IR (KBr): 3400, 3360, 3210, 1576, 1499 cm−1; MS (EI) m/z 380 (M+, 100); Elemental Anal. Calcd. for C22H24N2O4: C, 69.47; H, 6.32; N, 7.37. Found: C, 69.24; H, 6.43; N, 7.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365231B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-08bbccc28a9a4eb49cdfb8577e60c31a |
| Source note | uspto-grants-2008_04 |