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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600842Generated: October 31, 2026

Trifluoroacetic acid → HCID 57667108, compound

https://huagongshe.com/reaction/600842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzaldehyde dimethyl acetalHCID 62375—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57667036HCID 57667036—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 57667108HCID 5766710877%

Reaction Steps

To a stirred solution of (S)-2,2-dimethyl-4-phenylaminomethyl-oxazolidine-3-carboxylic acid tert-butyl ester (495 mg; example 2.a) at r.t. in 1,2-dichloroethane (10 ml) under an argon atmosphere were added benzaldehyde dimethyl acetal (0.37 ml), trifluoroacetic acid (0.13 ml) and sodium triacetoxyborohydride (571 mg). The mixture was stirred at room temperature overnight. The mixture was directly adsorbed on silica gel and purified by chromatography (SiO2; gradient:heptane->heptane/EtOAc 7:3) to give (S)-4-[(benzyl-phenyl-amino)-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (492 mg, 77%) as a colourless viscous oil. MS (ISP): 397.4 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902238B2
Source datasetuspto-grants-2011_03
ORD IDord-f7fbe9662ad94f959c7f2301db999dbe
Source noteuspto-grants-2011_03