HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927781Generated: October 26, 2026
Benzyltrimethylammonium hydroxide → (Z)-N-(4-chlorophenethyl)-4-(4-(2-(methylsulfinyl)-2-(methylthio)vinyl)-2-(trifluoromethyl)phenoxy)benzamide
https://huagongshe.com/reaction/1927781
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| Reactant | N-(4-chlorophenethyl)-4-(4-formyl-2-(trifluoromethyl)phenoxy)benzamide | HCID 86643290 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Z)-N-(4-chlorophenethyl)-4-(4-(2-(methylsulfinyl)-2-(methylthio)vinyl)-2-(trifluoromethyl)phenoxy)benzamide | HCID 86643291 | 79.1% |
Reaction Steps
To a solution of N-(4-chlorophenethyl)-4-(4-formyl-2-(trifluoromethyl)phenoxy)benzamide (0.225 g, 0.502 mmol) in THF (5 ml) was added methylsulfinyl(methylthio)methane (0.125 g, 1.00 mmol) followed by benzyltrimethylammonium hydroxide (0.114 ml, 0.251 mmol) and the reaction was stirred at 70° C. fort hour. The reaction was cooled, loaded onto a silica gel sample and the product was eluted using a gradient of 0.5% methanol/dichloromethane to 15% methanol/dichloromethane. Isolated (Z)-N-(4-chlorophenethyl)-4-(4-(2-(methylsulfinyl)-2-(methylthio)vinyl)-2-(trifluoromethyl)phenoxy)benzamide (0.220 g, 79.0% yield) which by TLC appeared to be a 4:1 mixture of olefin isomers. The crude material was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183289B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-fbc22c7600f6423ba77595adfb8100ac |
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| Source note | uspto-grants-2012_05 |
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