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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799296Generated: October 30, 2026

Potassium Hydroxide → Tert-butyl (2s)-2-[(diphenylmethylene)amino]-3-[4-(trifluoromethoxy)phenyl]propanoate

https://huagongshe.com/reaction/1799296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1-(Bromomethyl)-4-(trifluoromethoxy)benzeneHCID 142785—
ReactantN-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
SolventTolueneHCID 1140—
ProductTert-butyl (2s)-2-[(diphenylmethylene)amino]-3-[4-(trifluoromethoxy)phenyl]propanoateHCID 9097328088%

Reaction Steps

1-(Bromomethyl)-4-(trifluoromethoxy)benzene (28.1 g, 0.110 mol) and 50% potassium hydroxide (225 mL, 2.00 mol) were added to a toluene (1 L) suspension of tert-butyl [(diphenylmethylene)amino]acetate (29.5 g, 0.10 mol) and N-(9-anthracenylmethyl)cinchonidinium chloride (5.79 g, 0.01 mol) under ice-cooling with stirring. The mixture was vigorously stirred at the same temperature for 3.25 hours and then separated into an organic layer and an aqueous layer. The aqueous layer was extracted with ethyl acetate (200 mL), and the organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate, 20:1, 15:1, and 10:1, V/V) to give 41.2 g of the title compound (mixture of a yellow oil and a yellow solid, yield: 88%, optical purity: 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344029B2
Source datasetuspto-grants-2013_01
ORD IDord-ae47d7660b0243dcae19fec997736c8d
Source noteuspto-grants-2013_01