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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16576Generated: October 26, 2026

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

https://huagongshe.com/reaction/16576

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 numberUS07737163B2
Source datasetuspto-grants-2010_06
ORD IDord-cf6451dbc6644fd1a0ae0403fdb3b195
Source noteuspto-grants-2010_06