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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241519Generated: October 25, 2026

Water → 4-bromo-3-chloro-N-trimethylsilanylmethyl-thiobenzimidic acid methyl ester

https://huagongshe.com/reaction/241519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant4-bromo-3-chloro-N-trimethylsilanylmethylthiobenzamideHCID 86685705—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-3-chloro-N-trimethylsilanylmethyl-thiobenzimidic acid methyl esterHCID 6683665976.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 4-bromo-3-chloro-N-trimethylsilanylmethyl-thiobenzamide (10.40 g, 30.88 mmol) in THF (200 mL) was added methyl iodide (5.77 mL, 13.15 g, 92.7 mmol) and Cs2CO3 (30.19 g, 92.7 mmol) at −5° C. After 1 h at this temperature, the mixture was heated at 40° C. and stirred over night. Water was added and the mixture was extracted three times with MTBE. The combined organic phases were dried over Na2SO4, filtered and concentrated in vacuum. The residue was purified by filtration over a short plug of silica gel to give the title compound (8.25 g), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653000B2
Source datasetuspto-grants-2014_02
ORD IDord-c293342cb2f44c8c9470e59173be86d6
Source noteuspto-grants-2014_02