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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711171Generated: October 27, 2026

Imidazole → 5-Iodo-2-triisopropylsilanyloxy-benzoic acid methyl ester

https://huagongshe.com/reaction/711171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriisopropylsilyl chlorideHCID 139400—
ReactantMethyl 5-IodosalicylateHCID 248910—
SolventDimethylformamideHCID 6228—
Product5-Iodo-2-triisopropylsilanyloxy-benzoic acid methyl esterHCID 12337187492.1%

Reaction Steps

A solution of methyl 5-iodosalicylate (2.00 g, 7.20 mmol) in DMF (20 mL) was treated with imidazole (1.22 g, 18.0 mmol) then chlorotriisopropylsilane (1.85 mL, 8.60 mmol). The mixture was stirred at RT for 18 h. The mixture was evaporated in vacuo and the residue was partitioned between EtOAc and water. The aqueous layer was then extracted with EtOAc (2×). The combined organic layers were washed with a 10% aqueous citric acid solution, 1N aqueous NaOH solution and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified by FCC, using 0-10% EtOAc in cyclohexane, to give the title compound as a colorless oil (2.88 g, 92%). LCMS (Method 3): Rt 5.72 min, m/z 435 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181242B2
Source datasetuspto-grants-2015_11
ORD IDord-4e8ed11e90284f3098a6ba0e91bc1a8e
Source noteuspto-grants-2015_11