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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114486Generated: October 30, 2026

Acetic Acid → HCID 59809564, compound

https://huagongshe.com/reaction/2114486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59809535HCID 59809535—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
SolventEthyl AcetateHCID 8857—
ProductHCID 59809564HCID 5980956446%

Reaction Steps

To a solution of 4-amino-3-(2-bromophenoxy)-benzonitrile, 2a (0.8 g; 2.77 mmol) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (1.1 g; 5.52 mmol) in dichloroethane (80 mL) was added sodium triacetoxyborohydride (1.17 g; 5.52 mmol) and acetic acid (0.16 mL; 2.8 mmol). The mixture was stirred for 2 h at rt. An additional 4 equiv of sodium triacetoxyborohydride was added, and the mixture was heated to 90° C. for 5 h. The mixture was allowed to cool to rt, diluted with ethyl acetate (15 mL) and treated with H2O (15 mL). The organic layer was separated, dried over MgSO4, filtered, and evaporated. The residue was purified via column chromatography (eluent gradient: 0 to 30% ethyl acetate in heptane) to yield 0.6 g (46%) of 4-[2-(2-bromophenoxy)-4-cyanophenylamino]-piperidine-1-carboxylic acid tert-butyl ester, 3a. MS m/z (MH+) 493.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432257B2
Source datasetuspto-grants-2008_10
ORD IDord-f6cc9bd5ca24430dad9afa2850736cc9
Source noteuspto-grants-2008_10