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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555764Generated: October 31, 2026

Bromoacetonitrile → 2-[4-(2-Methoxy-ethoxy)-piperidin-1-yl]-acetonitrile

https://huagongshe.com/reaction/555764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
Reactant4-(2-Methoxyethoxy)piperidineHCID 14022384—
Product2-[4-(2-Methoxy-ethoxy)-piperidin-1-yl]-acetonitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053457B2
Source datasetuspto-grants-2011_11
ORD IDord-50ceab4ebf8b4b0e96a3d65aa083611a
Source noteuspto-grants-2011_11