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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252395Generated: November 4, 2026

3-Phenoxybenzaldehyde → HCID 16735089, compound

https://huagongshe.com/reaction/2252395

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenoxybenzaldehydeHCID 38284—
ReactantHCID 178506676HCID 178506676—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16735089HCID 1673508986%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 3-phenoxybenzaldehyde (2 g, 10.09 mmol) in THF (15 mL) at −78° C. was added phenyllithium (6.73 mL, 1.8M solution in cyclohexane-ether) dropwise. After stirring under argon at −78° C. for 4 hrs, the reaction was quenched with water and extracted with diethyl ether. The organic layer was washed with brine, dried with magnesium sulfate, filtered, and concentrated under reduced pressure to give the crude product. The crude mixture was purified via flash SiO2 chromatography (ethyl acetate/hexanes (10%/90%) to (20%/80%)) to give 128 (2.79 g, 86% yield): 1H-NMR (400 MHz, chloroform-d) δ 6.87-7.38 (m, 10 H), 7.09 (m, 1 H), 6.99 (app d, J=7.3 Hz, 1 H), 6.88 (m, J=8.6, 2.2 Hz, 1 H), 5.81 (s, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07321065B2
Source datasetuspto-grants-2008_01
ORD IDord-840552ad1fd648fe9486318667412602
Source noteuspto-grants-2008_01