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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592284Generated: October 30, 2026

tert-Butylsulfinamide, (R)-(+)- → (NZ)-2-methyl-N-[[2-(trifluoromethyl)pyrimidin-5-yl]methylidene]propane-2-sulfinamide

https://huagongshe.com/reaction/592284

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
Reactant2-(Trifluoromethyl)pyrimidine-5-carbaldehydeHCID 17750941—
CatalystCopper SulfateHCID 24462—
Solvent1,1-DichloroethaneHCID 6365—
Product(NZ)-2-methyl-N-[[2-(trifluoromethyl)pyrimidin-5-yl]methylidene]propane-2-sulfinamideHCID 8709453098.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-(trifluoromethyl)pyrimidine-5-carbaldehyde (27.2 g, 99 mmol) in dichloroethane (250 mL) was added (R)-(+)-2-methyl-2-propanesulfinamide (13.3 g, 109.0 mmol) and copper(II) sulfate (31.5 g, 197.0 mmol). The mixture was heated to 50° C. After 18 h, the mixture was cooled to ambient temperature and filtered through a pad of silica gel. The filtered cake was washed with dichloromethane and the filtrate was concentrated to give the title compound (27.3 g). MS 224 [(M+1)-56].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238647B2
Source datasetuspto-grants-2016_01
ORD IDord-7c4af7ccee1c4865b328fd0603dd5b2c
Source noteuspto-grants-2016_01