Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645963Generated: October 26, 2026

Tert-butyl 4-cyanooxane-4-carboxylate → Tert-butyl 4-(aminomethyl)oxane-4-carboxylate

https://huagongshe.com/reaction/645963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-cyanooxane-4-carboxylateHCID 23131610—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductTert-butyl 4-(aminomethyl)oxane-4-carboxylateHCID 6723283483%

Reaction Steps

A mixture of tert-butyl 4-cyanotetrahydro-2H-pyran-4-carboxylate (18.95 g, 0.0897 mol, step 1) and Raney Ni (1.00 g) in methanol (200 mL) was hydrogenated (3 atm) at room temperature for 12 h. Then, the mixture was filtered through a pad of Celite, and the filtrate was concentrated in vacuo to give 16.01 g (83%) of the title compound as a yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705020B2
Source datasetuspto-grants-2010_04
ORD IDord-365e79b8a35040178f91116075c13185
Source noteuspto-grants-2010_04