Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41320Generated: October 26, 2026

Benzaldehyde → 1,2-Diphenylethanol

https://huagongshe.com/reaction/41320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 178419663HCID 178419663—
SolventSodium SulfateHCID 24436—
Product1,2-DiphenylethanolHCID 94178—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To 100 mL (0.10 mol) of 1.0 M BnMgBr in THF 9.50 g (90 mmol) of benzaldehyde (2) was added with vigorous stirring at −10° C. This mixture was slowly warmed to room temperature and then stirred for 2 hr at this temperature. The mixture was added to 300 mL of saturated aqueous Na2SO4. The organic layer was separated and washed with saturated aqueous NH4Cl. The aqueous layer was extracted with 2×100 mL of diethyl ether. The combined organic extracts were evaporated to dryness, and the residue was dissolved in 100 mL of dichloromethane. The obtained solution was dried over Na2SO4 and evaporated to dryness. This crude product was further used without an additional purification. Yield 12.0 g (67%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530593B2
Source datasetuspto-grants-2013_09
ORD IDord-a92efe51f65c46a4a278f1dc879cb1d8
Source noteuspto-grants-2013_09