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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965459Generated: October 25, 2026

Butyl iodide → 2',3'-Di-n-butoxy-2,6-dichloro-4'-methoxy-6'-methyl-benzophenone

https://huagongshe.com/reaction/965459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantSodium hydrideHCID 24758—
Reactant2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenoneHCID 54569551—
SolventTetrahydrofuranHCID 8028—
Product2',3'-Di-n-butoxy-2,6-dichloro-4'-methoxy-6'-methyl-benzophenoneHCID 53713925—

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodiumhydride (0.4 g; 60%; 10 mmol) is added with stirring to a solution of 2,6-dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone (1.64 g; 5 mmol) in tetrahydrofurane. The solvent is evaporated and the residue dissolved in 30 ml of dimethylformamide. 1-iodo-n-butane (4.6 g; 25 mmol) is added, the mixture is stirred at 100° C. for 8 hours and then the solvent is evaporated. The residue is shaken with toluene/2N hydrochloric acid, the organic layer separated, washed with water and the solvent evaporated. The residue is purified by chromatography (flash column filled with 35 g of silicagel; elution with 500 ml of petrolether containing 2% of ethylacetate); yellow oil (0.7 g; 32% y).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773663
Source datasetuspto-grants-1998_06
ORD IDord-1c3f43f7342345d3bbb71eabe79c1ab1
Source noteuspto-grants-1998_06