HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076844Generated: October 26, 2026
Aniline → Tribromophenol Triphenylphosphite Aniline Propylene Oxide Triethylamine
https://huagongshe.com/reaction/1076844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Reactant | Phenol, tribromo- | HCID 32928 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Tribromophenol Triphenylphosphite Aniline Propylene Oxide Triethylamine | HCID 86733448 | — |
Reaction Steps
A 1-liter flask, standardly equipped, was charged with 331 grams of tribromophenol containing between 700 and 800 ppm of aluminum and ferric compounds, 46.5 grams of aniline and 180 grams of triphenylphosphite. After heating the mixture to 130°C., 145 ml. of propylene oxide was added at a temperature up to 155°C. After cooling, 5 grams of triethylamine was added followed by the addition of 80 ml. of propylene oxide at approximately 80°C. The mixture was then stripped of volatile materials at 80°C./1 mm. Hg to remove volatiles. There remained as residue 632.8 grams of oxypropylated product having a hydroxyl number of 170, an acid number of 1.9 and the product contained 38.5 percent bromine and 2.8 percent phosphorus.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03957922 |
|---|
| Source dataset | uspto-grants-1976_05 |
|---|
| ORD ID | ord-04a8b995433643c7865391ea4a5fd188 |
|---|
| Source note | uspto-grants-1976_05 |
|---|