HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → (1-Thiocarbamoylpiperidin-4-yl)acetic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Fmoc isothiocyanate | HCID 4154759 | — |
| Reactant | Tert-butyl 2-(piperidin-4-yl)acetate | HCID 23511620 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (1-Thiocarbamoylpiperidin-4-yl)acetic acid tert-butyl ester | HCID 58706572 | — |
Reaction Steps
A solution of piperidin-4-ylacetic acid tert-butyl ester (10.72 g, 50.0 mmol) in chloroform (100 ml) was added to a solution of 9-fluorenylmethoxycarbonyl isothiocyanate (14.07 g, 50.0 mmol) in chloroform (100 ml) and the mixture was stirred at room temperature for 1 hour. Then, piperidine (80 ml) was added and the mixture was stirred at room temperature for 30 minutes. After the reaction solution was concentrated, water was added, and it was extracted with ethyl acetate and washed with a saturated brine. The organic layer was dried over magnesium sulfate and the residue obtained by vacuum concentration was washed with isopropyl ether and the title compound was obtained (11.35 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803801B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-0ca6a52373b042fbb4b75bbd76010b49 |
| Source note | uspto-grants-2010_09 |