HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 437452Erstellt: 24. Oktober 2026
Antimony pentachloride → 1-Bromo-3-(heptafluoropropyl)benzene
https://huagongshe.com/de/reaction/437452
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Antimony pentachloride | HCID 24294 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Chlorine | HCID 24526 | — |
| Edukt | (Heptafluoropropyl)benzene | HCID 13418746 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-Bromo-3-(heptafluoropropyl)benzene | HCID 21428428 | — |
Reaktionsschritte
First meta-bromo(heptafluoropropyl)benzene is prepared as follows. 12 g (0.04 mole) of antimony pentachloride are added to 389 g (1.58 mole) of heptafluoropropylbenzene and then, with intensive stirring, 41 ml (0.79 mole) of bromine are added in drops within an hour with simultaneously cooling the reaction mixture on a water bath. The temperature of the reaction mixture is maintained at 26° C maximum. After adding all the bromine, the reaction mixture is given another stirring for 15 minutes. In the course of the entire bromination reaction, dry chlorine is passed into the reaction mixture at a rate of 3 liters per hour. On completion of the reaction, for binding the unreacted bromine, the reaction mixture is poured into 500 ml of water containing 25 ml of saturated solution of sodium bisulphite. The reaction product is distilled with steam, neutralized with a 5 percent solution of sodium hydroxide dried over calcined calcium chloride, and rectified. The yield of meta-bromo(heptafluoropropyl)benzene is 447.2 g (87 percent of theory).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04031119 |
|---|
| Quelldatensatz | uspto-grants-1977_06 |
|---|
| ORD ID | ord-3e31385bf48f4be7a2ae10e4976f962d |
|---|
| Quellennotiz | uspto-grants-1977_06 |
|---|