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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253390Generated: November 2, 2026

4-Iodobenzoyl chloride → HCID 25127626, compound

https://huagongshe.com/reaction/1253390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodobenzoyl chlorideHCID 74373—
ReactantAminopropyltrimethoxysilaneHCID 83756—
SolventDichloromethaneHCID 6344—
ProductHCID 25127626HCID 25127626—

Reaction Steps

4-Iodo-N-[3-(trimethoxysilyl)propyl]-benzamide (1) was prepared, as illustrated in FIG. 5, where a solution of 3-aminopropyltrimethoxysilane (1.78 mL, 10 mmol) in 10 mL of dichloromethane was added dropwise to a suspension of 4-iodobenzoyl chloride (1.33 g, 5 mmol) in 20 mL of dichloromethane at 0° C. The mixture was stirred for 1 hour and solvent was evaporated in vacuo. The residue was purified by column chromatography on silica using 2% methanol in chloroform. The solvent was removed by rotary evaporation to give a viscous oil. 1H NMR (300 MHz, CDCl3): δ 0.70 (t, J=8.1 Hz, 2H), 1.73 (m, 2H), 3.42 (m, 2H), 6.64 (br, 1H), 7.49 (d, J=8.7 Hz, 2H), 7.76 (d, J=8.7 Hz, 2H). 13C NMR (75 MHz, CDCl3): δ 6.81, 22.78, 42.54, 50.89, 98.41, 128.78, 134.44, 137.91, 167.03. HRMS calculated for C13H20INO4Si 409.0206, found 410.0295 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455265B2
Source datasetuspto-grants-2013_06
ORD IDord-bd5bc1dda0664f6697e9d4323fc3e08c
Source noteuspto-grants-2013_06