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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195484Generated: October 30, 2026

Water → FMOC-Ser(O-Bzl) oxazolidin-4-one

https://huagongshe.com/reaction/1195484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantFmoc-O-benzyl-L-serineHCID 7017914—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductFMOC-Ser(O-Bzl) oxazolidin-4-oneHCID 131717342—

Reaction Steps

A suspension of FMOC-Ser(O-Bzl) (4.16 g), paraformaldahyde (2.0 g), and p-toluenesulfonic acid (0.2 g) in toluene (400 ml) was heated under reflux with azeotropic water removal for 45 min. The solution was cooled, diluted with ethyl acetate (250 ml) and washed three times with 5% aqueous NaHCO3, dried (Na2SO4), and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with (8:2) hexane:ethyl acetate to give FMOC-Ser(O-Bzl)-oxazolidin-4-one as a crystalline product, m.p. 108°-109° C. Fab Mass spec. m/e 430(M+H)+. FMOC-Ser-(O-Bzl)-oxazolidin-4-one (3.14 g) was dissolved in chloroform (40 ml) and trifluoroacetic acid (40 ml) and triethylsilane (2.55 g) was added. The solution was stirred at room temperature for 22 hours, then concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with (95:5) methylene chloride:methanol to give FMOC-N-Me-Ser(O-Bzl)-OH as a colorless oil. Fab Mass spec., m/e 432 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110904
Source datasetuspto-grants-1992_05
ORD IDord-eadd23d9e90b46c7ab82c821cad42542
Source noteuspto-grants-1992_05