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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870933Generated: October 27, 2026

N-(Diphenylmethylene)glycine tert-butyl ester → HCID 86695928, compound

https://huagongshe.com/reaction/870933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
ReactantLithium diisopropylamideHCID 2724682—
Reactant3,3,3-Trifluoropropyl trifluoromethanesulfonateHCID 14132849—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86695928HCID 8669592860%

Reaction Steps

To a stirred solution of tert-butyl 2-((diphenylmethylene)amino)acetate (1 g, 3.39 mmol) in THF (20 ml) cooled to −78° C. under nitrogen atmosphere was added LDA, 2M in THF/heptane/ethylbenzene (2.54 ml, 5.08 mmol) dropwise for 30 mins. To this mixture was then added 3,3,3-trifluoropropyl trifluoromethanesulfonate (1.083 g, 4.40 mmol). The reaction was gradually warmed to rt and stirred for 4 h. The reaction mixture was quenched by addition of saturated aqueous ammonium chloride at 0° C. The reaction mixture was then extracted with ethyl acetate (3×10 mL). The combined organic extracts were washed with water and brine, dried over sodium sulfate and then concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using 2% ethyl acetate in hexane to afford tert-butyl 2-((diphenylmethylene)amino)-5,5,5-trifluoropentanoate (800 mg, 2.02 mmol, 60% yield) as a yellow oil. LCMS (ESI) m/e 391.9 [(M+H)+, calcd for C22H24F3NO2, 392.2]; LC/MS retention time (method E): tR=2.49 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969564B2
Source datasetuspto-grants-2015_03
ORD IDord-6d48bc4ef7424bfd93b117474a955710
Source noteuspto-grants-2015_03