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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196456Generated: October 30, 2026

3'-Bromoacetophenone → 2-(3-Bromophenyl)propan-2-ol

https://huagongshe.com/reaction/2196456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-BromoacetophenoneHCID 16502—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventButyl etherHCID 8909—
Product2-(3-Bromophenyl)propan-2-olHCID 15072383—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under an argon stream, 6.5 g of 3-bromoacetophenone are placed in a round-bottomed flask and dissolved in 544 ml of diethyl ether and 272 ml of tetrahydrofuran. The mixture is cooled to 0° C. using an ice bath, and 100 ml of a 1M solution of methylmagnesium bromide in dibutyl ether are added thereto, dropwise. The mixture is stirred at 0° C. for 1 h and 400 ml of a saturated aqueous solution of ammonium chloride are added. The organic phase is separated, dried over magnesium sulphate and concentrated under reduced pressure. 10.0 g of compound are obtained. 1H NMR (DMSO-d6, δ in ppm): 1.45 (s, 6H); 5.15 (s, 1H); 7.25 (t, 1H); 7.4 (d, 1H); 7.45 (d, 1H); 7.65 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338451B2
Source datasetuspto-grants-2012_12
ORD IDord-b045dd1ce6884783a0ad8783d49cafee
Source noteuspto-grants-2012_12