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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
ReactantN-(4-chlorophenethyl)-4-(4-formyl-2-(trifluoromethyl)phenoxy)benzamideHCID 86643290—
SolventTetrahydrofuranHCID 8028—
Product(Z)-N-(4-chlorophenethyl)-4-(4-(2-(methylsulfinyl)-2-(methylthio)vinyl)-2-(trifluoromethyl)phenoxy)benzamideHCID 8664329179.1%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183289B2
Source datasetuspto-grants-2012_05
ORD IDord-fbc22c7600f6423ba77595adfb8100ac
Source noteuspto-grants-2012_05