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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437452Generated: October 27, 2026

Antimony pentachloride → 1-Bromo-3-(heptafluoropropyl)benzene

https://huagongshe.com/reaction/437452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAntimony pentachlorideHCID 24294—
ReactantBromineHCID 24408—
ReactantChlorineHCID 24526—
Reactant(Heptafluoropropyl)benzeneHCID 13418746—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
Product1-Bromo-3-(heptafluoropropyl)benzeneHCID 21428428—

Reaction Conditions

Temperature26 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031119
Source datasetuspto-grants-1977_06
ORD IDord-3e31385bf48f4be7a2ae10e4976f962d
Source noteuspto-grants-1977_06