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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535305Generated: October 30, 2026

1-(4-Iodophenyl)ethan-1-one → HCID 71145829, compound

https://huagongshe.com/reaction/535305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Iodophenyl)ethan-1-oneHCID 72869—
ReactantHCID 178490745HCID 178490745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71145829HCID 71145829—

Reaction Steps

A solution of 4-iodoacetophenone (2 g, 7.97 mmol) in THF (20 ml) was immersed in an ice-bath and (3-methoxyphenyl)magnesium bromide 1M in THF (23.90 ml, 23.90 mmol) was added slowly by syringe. The reaction mixture was stirred at r.t. for 3 hrs. The reaction mixture was quenched with 20 ml aqueous saturated NH4Cl solution and diluted with ethyl acetate. The organic phase was separated and washed with brine. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo to obtain the crude product which was purified by automated column chromatography (n-heptane (isom. mixture)/ethyl acetate). Organic solvents were removed to obtain title compound as yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859535B2
Source datasetuspto-grants-2014_10
ORD IDord-ad60ea66fbb84fabafd3f8657ce3f420
Source noteuspto-grants-2014_10