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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713401Generated: October 31, 2026

Trimethylsilyl iodide → HCID 59463816, compound

https://huagongshe.com/reaction/1713401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 59463818HCID 59463818—
SolventChloroformHCID 6212—
ProductHCID 59463816HCID 5946381640.7%

Reaction Steps

560 mg (1.7 mmol) of ethyl 3-(1-methoxy-5,6,7,8-tetrahydroisoquinolin-4-ylamino)benzoate (compound 12) are dissolved in 30 ml of chloroform and, at room temperature, 413 mg (2.1 mmol) of trimethylsilyl iodide are added. The mixture is then heated to reflux until complete conversion is reached by means of LCMS. Further trimethylsilyl iodide is added if necessary. For workup, the mixture is washed twice with H2O, dried with Na2SO4 and concentrated. Chromatography on silica gel (CH2Cl2/MeOH 95:5) affords 216 mg of the title compound. Yield: 40%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795278B2
Source datasetuspto-grants-2010_09
ORD IDord-d6c1ceb93baf4ecc89d6db11ec1d6e6e
Source noteuspto-grants-2010_09