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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818678Generated: November 2, 2026

Benzophenone → 1,1,2-Triphenylethanol

https://huagongshe.com/reaction/1818678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantBenzyl BromideHCID 7498—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product1,1,2-TriphenylethanolHCID 24501365%

Reaction Steps

To a suspension of Mg (1.7 g, 0.07 mol) in dry ether (25 mL) was added a solution of benzyl bromide (10 mL, 1.5 equ.) in dry ether (25 mL) drop-wise and allowed to stir at RT for 1 h. By the time all magnesium was dissolved and the reaction mixture was cooled to 0° C. To this was added a solution of benzophenone (10 g, 0.05 mol) in dry ether (25 mL) and allowed to stir at RT for 5 h. The progress of the reaction was followed by TLC and when it was ready the reaction mixture was quenched with saturated NH4Cl solution, extracted with ether (100 mL), washed with brine, dried and concentrated under vacuum. The crude product was purified by column chromatography on silica gel (10% ethyl acetate in pet. ether) to give the title compound (9.6 g, 65%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601702B2
Source datasetuspto-grants-2009_10
ORD IDord-9310c1c629d2486791e3c880ee4703e7
Source noteuspto-grants-2009_10