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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284191Generated: October 31, 2026

Benzene, 1-bromo-3-(trifluoromethyl)- → HCID 23039573, compound

https://huagongshe.com/reaction/1284191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 21488082HCID 21488082—
SolventDiethyl EtherHCID 3283—
ProductHCID 23039573HCID 23039573—

Reaction Steps

The Grignard reagent prepared from 14.5 g. (0.6 mole) of magnesium and 136 g. (0.6 mole) of m-bromobenzotrifluoride in 800 ml. of dry ether was cooled to -30°C. and treated with 53.5 g. (0.296 mole) of crude cyclopropyl 2-piperidinylethyl ketone in 200 ml. of ether at a rate that the temperature was maintained below -20°C. After addition, the mixture was stirred and allowed to warm to room temperature over a one-hour period. The reaction mixture was treated with 32 g. of ammonium chloride in 170 ml. of water and the ether layer was separated. The remainder of the reaction mixture was filtered and the resulting solid precipitate was extracted with 200 ml. portions of ether. The combined ether extracts were dried over magnesium sulfate and concentrated to an oil. The oil was distilled under reduced pressure and the distillate was converted to the hydrochloride salt. Recrystallization from acetone-ethanol mixture gave 3.6 g. (17%) of pure product which melted at 193°-194°C. after drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978129
Source datasetuspto-grants-1976_08
ORD IDord-48bda6d079794d7ea402b09d6d1eb740
Source noteuspto-grants-1976_08