HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → Ethyl 3-(1-Boc-2-pyrrolidinyl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57264746 | HCID 57264746 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(1-Boc-2-pyrrolidinyl)acrylate | HCID 53933727 | 132.2% |
Reaction Steps
To a stirred solution of (S)-2-(2-ethoxycarbonyl-vinyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (103 mg, 0.382 mmol) in THF (2 ml) was added EtSH (85 μl, 1.15 mmol) and NaH (60% in paraffin liquid: 46 mg, 1.15 mmol) at 0° C. The mixture was allowed to warm to room temperature and stirred for 7 hr. The mixture was quenched with 1N HCl, extracted with AcOEt, washed with saturated aqueous NaCl, dried (MgSO4), and concentrated in vacuo to give 2-(2-ethoxycarbonyl-vinyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (136 mg) as a crude oil, which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06737409B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-64ff5eb72b734d01b222758d2c56088f |
| Source note | uspto-grants-2004_05 |