Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793236Generated: October 25, 2026

2-Methyl-2-phenylpropanal → (S)-N-(2-Methyl-2-phenylpropylidene)-p-toluenesulfinamide

https://huagongshe.com/reaction/1793236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-phenylpropanalHCID 283879—
Reactant2,2-Dimethyl-3-phenyloxiraneHCID 5743355—
Reactant(S)-4-methylbenzenesulfinamideHCID 11116285—
CatalystTitanium tetraethoxideHCID 76524—
CatalystTris(pentafluorophenyl)boraneHCID 582056—
SolventBenzeneHCID 241—
Product(S)-N-(2-Methyl-2-phenylpropylidene)-p-toluenesulfinamideHCID 6962567181%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 2.5 g of 2,2-dimethyl-3-phenyloxirane (16 mmol) in 85 mL of anhydrous benzene is added 0.415 g (0.362 mmol, 5 mol %) of tris(pentafluorophenyl) borane. The light yellow solution is stirred at 25° C. for 19 hours. The reaction mixture containing the 2-methyl-2-phenylpropanal is then treated with (S)-p-toluenesulfinamide (2.3 g, 15 mmol) followed by a solution of 16 mL (73 mmol) titanium ethoxide in 155 mL of benzene. The yellow solution is stirred at 25° C. for 24 hours then cooled to 5–10° C. and quenched with 245 mL of water. The mixture is filtered through diatomaceous earth, and the filter cake washed with methylene chloride (4×50 mL). The aqueous layer is washed with methylene chloride (1×25 mL). The combined organic layers are dried (MgSO4) and concentrated under reduced pressure to give 3.74 g (81%) of the desired product as a white solid. The product is used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078572B2
Source datasetuspto-grants-2006_07
ORD IDord-02dcb73ac3424272a81fdd4037603a1a
Source noteuspto-grants-2006_07