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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-bromo-3-chloro-N-trimethylsilanylmethylthiobenzamide | HCID 86685705 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-bromo-3-chloro-N-trimethylsilanylmethyl-thiobenzimidic acid methyl ester | HCID 66836659 | 76.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653000B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-c293342cb2f44c8c9470e59173be86d6 |
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| Source note | uspto-grants-2014_02 |
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