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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3-IodobenzaldehydeHCID 252610—
Reactant2-Methylbenzene-1-sulfinic acidHCID 12661295—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
Solventtert-Butyl methyl etherHCID 15413—
Product{(3-Iodophenyl)[(4-methylphenyl)sulfonyl]methyl}formamideHCID 8592970351%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476677B2
Source datasetuspto-grants-2009_01
ORD IDord-2952c69dbed74c24843dae4c8ba792e7
Source noteuspto-grants-2009_01