HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → tert-Butyl 3-ethynylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | tert-Butyl 3-(2,2-dibromovinyl)piperidine-1-carboxylate | HCID 86615128 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 3-ethynylpiperidine-1-carboxylate | HCID 21963855 | 93% |
Reaction Steps
To a solution of 3-(2,2-Dibromo-vinyl)-piperidine-1-carboxylic acid tert-butyl ester (0.15 g, 0.42 mmol) in THF (1 ml) wad added at −78° C., 0.5 ml of n-BuLi 2.5 M in hexane (1.23 mmol). After 1 h at −78° C., the reaction mixture was quenched with 1 ml of water and the aqueous phase was extracted with AcOEt. The combined organic phase was dried over K2CO3, filtered and evaporated to give 80 mg (93%) of 3-Ethynyl-piperidine-1-carboxylic acid tert-butyl ester as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163775B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-fdfff796e719446c9c6442be03098baf |
| Source note | uspto-grants-2012_04 |