HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isocyanate → N-(t-butylaminocarbonyl)-beta-phenyl isoserine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isocyanate | HCID 62412 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | (2R,3S)-3-Phenylisoserine methyl ester | HCID 10176516 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(t-butylaminocarbonyl)-beta-phenyl isoserine methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06177573B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-d7eb527d984d4553a109ba50bc51fa36 |
| Source note | uspto-grants-2001_01 |