HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetonitrile → 2-[4-(2-Methoxy-ethoxy)-piperidin-1-yl]-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 4-(2-Methoxyethoxy)piperidine | HCID 14022384 | — |
| Product | 2-[4-(2-Methoxy-ethoxy)-piperidin-1-yl]-acetonitrile | HCID 86641794 | — |
Reaction Steps
The title compound is synthesized by coupling of 4-(2-Methoxy-ethoxy)-piperidine (commercially available from ChemBridge Corporation) and bromoacetonitrile analogously to the preparation of intermediate 149.2 as a colorless oil; ES-MS: M+=199.2; 1HNMR(DMSO-d6) 3.65 (s, 2H), 3.50 (dd, 2H), 3.40 (dd, 2H), 3.30-3.25 (m, 1H), 3.20 (s, 3H), 2.70-2.60 (m, 2H), 2.25-2.20 (m, 2H), 1.85-1.80 (m, 2H), 1.50-1.40 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08053457B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-50ceab4ebf8b4b0e96a3d65aa083611a |
| Source note | uspto-grants-2011_11 |