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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372583Generated: October 31, 2026

Trifluoroacetic acid → methyl 4-((2S,4S)-4-(2-naphthyloxy)-2-pyrrolidinylmethoxy)benzoate

https://huagongshe.com/reaction/1372583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantmethyl 4-((2S,4S)-1-tert-butoxycarbonyl-4-(2-naphthyloxy)-2-pyrrolidinylmethoxy)benzoateHCID 16093646—
SolventDichloromethaneHCID 6344—
Productmethyl 4-((2S,4S)-4-(2-naphthyloxy)-2-pyrrolidinylmethoxy)benzoateHCID 16093586114.2%

Reaction Steps

Trifluoroacetic acid (6 ml) was added to a solution of methyl 4-((2S,4S)-1-tert-butoxycarbonyl-4-(2-naphthyloxy)-2-pyrrolidinylmethoxy)benzoate (870 mg, 1.74 mmol) in methylene chloride (24 ml). The resulting mixture was stirred overnight at room temperature. To the residue obtained by concentrating the reaction mixture under reduced pressure was added 1N NaOH under ice cooling to make the residue alkaline, followed by extraction with methylene chloride. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (silica gel: 100 g), whereby from hexane/ethyl acetate (2/1) eluate fractions, the title compound (750 mg, 100%) was obtained as a black oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-7aa56ac66aad418589a9cceb20539d01
Source noteuspto-grants-2007_01