HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908539Generated: October 29, 2026
Benzophenone → alpha,alpha-Diphenylbenzeneethanol
https://huagongshe.com/reaction/908539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha,alpha-Diphenylbenzeneethanol | HCID 245013 | 65% |
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 crudeproduct 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. TLC: Pet. ether/EtOAc, 9:1, Rf=0.4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017620B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-2cdd4fc76c624d69911032a506321494 |
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| Source note | uspto-grants-2011_09 |
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