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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106986Generated: October 30, 2026

tert-Butyl isocyanate → N-(t-butylaminocarbonyl)-beta-phenyl isoserine methyl ester

https://huagongshe.com/reaction/1106986

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl isocyanateHCID 62412—
ReactantIsocyanateHCID 105034—
Reactant(2R,3S)-3-Phenylisoserine methyl esterHCID 10176516—
SolventTetrahydrofuranHCID 8028—
ProductN-(t-butylaminocarbonyl)-beta-phenyl isoserine methyl esterHCID 22389502—

Reaction Steps

(2R,3S)-β-phenyl-isoserine methyl ester (4.35 g, 22 mM) is dissolved in dry THF (100 mL) and the flask cooled to 0°. To the mixture is added t-butyl isocyanate (2.8 mL, 25 mM). TLC after 15 minutes shows some starting material left so additional isocyanate (0.5 mL) is added. TLC after 1 hour shows no starting material so the solvent is concentrated under reduced pressure to give the title compound, NMR (CDCl3, TMS) 1.27, 3.43, 3.81, 4.34, 4.48, 5.27, 5.32, 7.29 and 7.34 δ; MS (FAB-High Res.) theory for C15H22N2O4 --H=295.1658, found=295.1663.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057452
Source datasetuspto-grants-2000_05
ORD IDord-70f6a443be814b49ae2ff65ee66640fa
Source noteuspto-grants-2000_05