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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856649Generated: November 1, 2026

Tetrahydrofuran → HCID 20707075, compound

https://huagongshe.com/reaction/1856649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantBenzyl (piperidin-4-ylmethyl)carbamateHCID 14809798—
Reactant2-(4-Oxo-piperidin-1-yl)-benzonitrileHCID 15512646—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 20707075HCID 20707075—

Reaction Steps

To a solution of 2-(4-oxo-piperidin-1-yl)-benzonitrile (5) (653 mg, 3.26 mmol) and 4 (890 mg, 3.58 mmol) in 40 ml of methanol was added 4 g of powdered 4 Å molecular sieves. The resulting suspension was stirred at room temperature for 24 hours. The suspension was subsequently acidified to pH 5 with acetic acid and a 1M solution of NaCNBH3 in THF (6.0 ml 5.6 mmol) was added slowly with a syringe pump over 24 hours. When the addition was complete, the solvent was removed in vacuo and the residue taken up in chloroform and filtered. The solution was then washed with 10% Na2CO3, dried over MgSO4, and the solvent removed in vacuo to give the crude amine. The crude product was purified by chromatography on silica gel (5% MeOH/CHCl3) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143750
Source datasetuspto-grants-2000_11
ORD IDord-2049a2390aff4b3186073485a048872e
Source noteuspto-grants-2000_11