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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609524Generated: October 26, 2026

Potassium Iodide → Methyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-Phenylacetate

https://huagongshe.com/reaction/1609524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant18-Crown-6HCID 28557—
ReactantMethyl 2-(2-bromophenyl)acetateHCID 8063364—
Reactant4-Tert-butyldimethylsilyloxymethyl-2-allylphenolHCID 19934838—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-PhenylacetateHCID 1993485165.4%

Reaction Steps

To a suspension of KH (1.3 eq) in DMF (1 mL) was added a solution of the product of Step C (157 mg, 0.566 mmol) in DMF (1 mL), followed by 18-crown-6 (30 mg; 0.2 eq). The reaction mixture was stirred for 5 minutes at room temperature. A solution of methyl 2-bromophenylacetate (168 mg, 0.735 mmol) in DMF (1 mL) was added, followed by a catalytic amount of potassium iodide. The reaction was heated to 80° C. for 0.5 hours then stirred at room temperature for 16 hours. After concentration in vacuo, the residue was partitioned between water and ethyl acetate. The combined organic layers were washed with water, brine, then dried (MgSO4). After filtration and concentration in vacuo, the residue was chromatographed on silica (MPLC, ethyl acetate/hexanes (5/95)) to afford 158 mg (66%) of the title compound (Rf =0.22, 5% ethyl acetate/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401745
Source datasetuspto-grants-1995_03
ORD IDord-5d493879c1da4411bfa82bc2dfa2911a
Source noteuspto-grants-1995_03