Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43656Generated: October 26, 2026

Allyl iodide → tert-Butyl 3-allyloxy-4,4-dimethoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/43656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-hydroxy-4,4-dimethoxypiperidine-1-carboxylateHCID 11425480—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 3-allyloxy-4,4-dimethoxypiperidine-1-carboxylateHCID 6840595593.6%

Reaction Steps

The same operation as in Example (90a) was performed using tert-butyl 3-hydroxy-4,4-dimethoxypiperidine-1-carboxylate (5.2 g, 20 mmol), sodium hydride (55% content, 1.31 g, 30 mmol), allyl iodide (5.03 g, 30 mmol) and DMF (50 mL). The residue was purified by column chromatography (elution solvent: hexane/ethyl acetate=10/1, 4/1, 2/1) to obtain 5.64 g of the title compound as a colorless oily substance (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-d65d2f6d90c6495c999358709ee0b259
Source noteuspto-grants-2013_09