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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308744Generated: October 31, 2026

Hydrochloric Acid → 3'-Chloropropiophenone

https://huagongshe.com/reaction/2308744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantDiethyl EtherHCID 3283—
ReactantEthyl BromideHCID 6332—
ReactantBenzonitrile, m-chloro-HCID 13015—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
Product3'-ChloropropiophenoneHCID 587128—

Reaction Steps

4.86 g (0.2 mol) of magnesium turnings, 30 ml of dry diethyl ether and a grain of iodine are placed in a one liter three-necked round-bottomed flask equipped with a condenser, a calcium chloride drying tube, a pressure equalizing funnel and a magnetic stirrer; the flask is purged with nitrogen, and 21.8 g (0.2 mol) of ethyl bromide in 30 ml of dry diethyl ether are then added. The mixture is then heated under reflux for one hour and left to cool. At ambient temperature, 16.51 g (0.12 mol) of 3-chlorobenzonitrile in 70 ml of dry diethyl ether are then added. A copious precipitate forms. The mixture is stirred overnight at ambient temperture and then cooled in an ice bath and hydrolysed by slowly adding 50 ml of water and then about 100 ml of 6N hydrochloric acid until the pH is acid. The mixture is stirred for one and a half hours and then extracted with ethyl acetate. The organic extract is then washed twice with water, dried and concentrated on a rotary evaporator. This gives 26 g of an orange oil, which is concentrated in vacuo to give about 18.2 g of ochre crystals of 3'-chloropropiophenone melting at about 40° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04690931
Source datasetuspto-grants-1987_09
ORD IDord-902fbf54239e4635b4818037a3292794
Source noteuspto-grants-1987_09