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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173777Generated: October 27, 2026

Dichloromethane → (NE,R)-2-methyl-N-[[4-[4-(trifluoromethyl)phenyl]phenyl]methylidene]propane-2-sulfinamide

https://huagongshe.com/reaction/2173777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
Reactant4'-(Trifluoromethyl)-4-biphenylcarbaldehydeHCID 2782712—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
CatalystTitaniumHCID 23963—
CatalystTitanium tetraethoxideHCID 76524—
SolventMethanolHCID 887—
Product(NE,R)-2-methyl-N-[[4-[4-(trifluoromethyl)phenyl]phenyl]methylidene]propane-2-sulfinamideHCID 8854023984%

Reaction Steps

A round bottom flask equipped with a condenser was charged with 4′-(trifluoromethyl)biphenyl-4-carbaldehyde (20.0 g, 79.9 mmol), (R)-(+)-2-methylpropane-2-sulfinamide (9.69 g, 79.9 mmol) and dichloromethane (400 mL). Titanium(IV) ethoxide (33.2 mL, 160 mmol) was then added, and the mixture was heated to reflux for 3 hours. Methanol (50 mL) and saturated sodium bicarbonate (10 mL) were then added to the reaction, causing the titanium salts to precipitate. This mixture was stirred for 30 minutes and then filtered, rinsing with ethyl acetate. Sodium sulfate was added to the filtrate to remove the water and then filtered a second time. The solvent was removed under reduced pressure to afford (R,E)-2-methyl-N-((4′-(trifluoromethyl)biphenyl-4-yl)methylene)propane-2-sulfinamide (23.7 g, 84%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 1.30 (s, 9H) 7.70-7.74 (m, 2H) 7.74 (s, 4H) 7.95-7.99 (m, 2H) 8.66 (s, 1H). MS (M+1): 354.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056834B2
Source datasetuspto-grants-2015_06
ORD IDord-53dbfb2869f341128625b5475b52f159
Source noteuspto-grants-2015_06