HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253390Generated: November 2, 2026
4-Iodobenzoyl chloride → HCID 25127626, compound
https://huagongshe.com/reaction/1253390
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Iodobenzoyl chloride | HCID 74373 | — |
| Reactant | Aminopropyltrimethoxysilane | HCID 83756 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25127626 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08455265B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-bd5bc1dda0664f6697e9d4323fc3e08c |
|---|
| Source note | uspto-grants-2013_06 |
|---|