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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600835Generated: October 30, 2026

Trifluoroacetic acid → HCID 57667096, compound

https://huagongshe.com/reaction/600835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-MethoxypropeneHCID 8300—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57667036HCID 57667036—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 57667096HCID 5766709689%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred solution of (S)-2,2-dimethyl-4-phenylaminomethyl-oxazolidine-3-carboxylic acid tert-butyl ester (650 mg) at r.t. in 1,2-dichloroethane (15 ml) under an argon atmosphere were added 2-methoxypropene (0.30 ml), trifluoroacetic acid (0.16 ml) and sodium triacetoxyborohydride (674 mg). The mixture was heated to 40° C. overnight. The mixture was cooled to r.t., directly adsorbed on silica gel and purified by chromatography (SiO2; gradient:cyclohexane->cyclohexane/EtOAc 7:3) to give (S)-4-[(isopropyl-phenyl-amino)-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (659 mg, 89%) as light yellow viscous oil. MS (ISP): 349.5 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902238B2
Source datasetuspto-grants-2011_03
ORD IDord-32363e059c7a4a23adf6d054826c7c0a
Source noteuspto-grants-2011_03