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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220596Generated: October 29, 2026

Benzyl Bromide → N-[(1S,2R)-2-(4-Benzyloxy-3-nitrophenyl)-2-hydroxy-1-methylethyl]-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/2220596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,2-Trifluoro-N-[(1S,2R)-2-hydroxy-2-(4-hydroxy-3-nitrophenyl)-1-methylethyl]acetamideHCID 86611764—
SolventDimethylformamideHCID 6228—
ProductN-[(1S,2R)-2-(4-Benzyloxy-3-nitrophenyl)-2-hydroxy-1-methylethyl]-2,2,2-trifluoroacetamideHCID 86611766—

Reaction Steps

Benzyl bromide (22 mL) was added to a suspension of 2,2,2-trifluoro-N-[(1S,2R)-2-hydroxy-2-(4-hydroxy-3-nitrophenyl)-1-methylethyl]acetamide (55 g) and potassium carbonate (36.8 g) in N,N-dimethylformamide (529 mL) at room temperature with stirring, and the mixture was stirred at 60° C. for 1 hr. The reaction mixture was concentrated in vacuo, and ethyl acetate and water were added to the residue. The organic layer was separated, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (73 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417169B2
Source datasetuspto-grants-2008_08
ORD IDord-aa21642c4c644e2f9e459bb387fe40ee
Source noteuspto-grants-2008_08