HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → HCID 57266187, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Piperidineethanol | HCID 73953 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57266187 | HCID 57266187 | 100% |
Reaction Steps
The title compound was prepared according to general procedure G described in Scheme 3. 2-(Piperidin-4-yl)ethanol (1.2 g, 9.3 mmol) was treated with 2-chloroacetonitrile (1.4 g, 18.6 mmol), triethylamine (10.4 mL, 74.3 mmol) and stirred at RT for 14 h. The crude reaction mixture was diluted with Et2O (25 mL) and washed with H2O (3×10 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford the title compound as a yellow oil (1.56 g, 100%), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114894B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-adf550375f0241da9941e8ecd8a40cf2 |
| Source note | uspto-grants-2012_02 |