HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453669Generated: October 27, 2026
Formamide → {(3-Iodophenyl)[(4-methylphenyl)sulfonyl]methyl}formamide
https://huagongshe.com/reaction/1453669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamide | HCID 713 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 3-Iodobenzaldehyde | HCID 252610 | — |
| Reactant | 2-Methylbenzene-1-sulfinic acid | HCID 12661295 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | {(3-Iodophenyl)[(4-methylphenyl)sulfonyl]methyl}formamide | HCID 85929703 | 51% |
Reaction Steps
Trimethylsilylchloride (9.1 mL) was added to a stirred solution of 3-iodobenzaldehyde (15.1 g) and formamide (6.5 mL) in MeCN (34 mL) and toluene (34 mL) under an inert atmosphere. The reaction was then heated at 50° C. for 5 hours. Toluene sulfinic acid (15.3 g) was added and the reaction mixture was heated at 50° C. for a further 5 hours. The reaction mixture was cooled to ambient temperature, methyl t-butylether (55 mL) was added and stirred for 5 minutes. Water (275 mL) was added, the reaction cooled to 0° C. and stirred for 1 hour. The solid was filtered and the reaction flask was washed with MTBE (2×35 mL) and poured over the filtered cake. The solid was dried in a vacuum oven at 60° C. for 10 hours to afford impure title compound as a solid (14 g, 51%) which was used without further purification. A small sample was crystallised from EtOH;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476677B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-2952c69dbed74c24843dae4c8ba792e7 |
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| Source note | uspto-grants-2009_01 |
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