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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845156Generated: October 31, 2026

Bromobenzene → HCID 54203413, compound

https://huagongshe.com/reaction/845156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 13672830HCID 13672830—
SolventDiethyl EtherHCID 3283—
ProductHCID 54203413HCID 5420341327.6%

Reaction Steps

A solution of bromobenzene (24.8 g) in ethyl ether (120 cc) is added dropwise over approximately 1 hour to a suspension of magnesium turnings (3.85 g) in ethyl ether (100 cc). 4-Dimethylamino-1-phenyl-2-butyn-1-ol (10 g) in ethyl ether (30 cc) is added over approximately 15 minutes to the black solution obtained. The reaction mixture is then refluxed for 3 hours and 30 minutes, and then poured into a mixture of ice (400 g) and a saturated aqueous solution (200 cc) of ammonium chloride. The organic phase is separated; the aqueous phase is extracted with methylene chloride (2×200 cc); the organic phases are combined, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. The residue is purified by "flash" chromatography [eluent: methanol/ethyl acetate (60/40 by volume)], fractions 18 to 39 are combined and concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. After the residue has been recrystallised from isopropyl ether, 4-dimethylamino-1,2-diphenyl-2-buten-1-ol (E) (3.9 g) is obtained in the form of white crystals melting at 113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04755599
Source datasetuspto-grants-1988_07
ORD IDord-347add163a2344c2886196447ec73815
Source noteuspto-grants-1988_07