HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (S)-2-(3-Ethoxycarbonylallyl)-piperazine-1,4-dicarboxylic acid di-tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | (S)-2-(2-Oxoethyl)piperazine-1,4-dicarboxylic acid di-tert-butyl ester | HCID 86604575 | — |
| Product | (S)-2-(3-Ethoxycarbonylallyl)-piperazine-1,4-dicarboxylic acid di-tert-butyl ester | HCID 69212154 | — |
Reaction Steps
Heat a mixture of (S)-2-(2-oxoethyl)-piperazine-1,4-dicarboxylic acid di-tert-butyl ester (1.38 g, 4.21 mmol) and (carbethoxymethylene)triphenylphosphorane (1.87 g, 5.38 mmol) in THF (17 mL) at reflux for 4 h. Concentrate the mixture under reduced pressure and purify by silica gel chromatography eluting with 20% to 50% EtOAc in hexanes. Combine the purified fractions, concentrate under reduced pressure, azeotrope with CH2Cl2/hexanes (1:2) and place under vacuum to give the title compound: yellow tar (0.961 g), mass spectrum (m/e): 416.09(M+NH4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384934B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-2a2c7e08130342ac8483f90771c8781f |
| Source note | uspto-grants-2008_06 |