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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782577Generated: November 1, 2026

Sodium Hydroxide → HCID 68975066, compound

https://huagongshe.com/reaction/1782577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Difluoromethoxy)anilineHCID 737363—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(betaR)-beta-Methyl-4-oxo-1-piperidinepropanenitrileHCID 68972438—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 68975066HCID 6897506676%

Reaction Steps

Following General Procedure A, a solution of 4-difluoromethoxyaniline (0.50 g, 3.1 mmol) and (R)-3-(4-oxo-piperidin-1-yl)-butyronitrile (0.44 g, 2.6 mmol) in CH2Cl2 (10 mL), was treated with glacial AcOH (3 drops) and NaBH(OAc)3 (0.83 g, 3.9 mmol), stirring for 16 h at room temperature. Saturated aqueous NaHCO3 solution (15 mL) and 1N NaOH (2 mL) was added and the phases were separated and the aqueous extracted with CH2Cl2 (2×15 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude material was then purified by flash column chromatography on silica gel (1:1 EtOAc/CH2Cl2) to afford (R)-3-[4-(4-difluoromethoxy-phenylamino)-piperidin-1-yl]-butyronitrile as a white solid (0.61 g, 76%). 1H NMR (CDCl3) δ 1.20 (d, 3H, J=6.6 Hz), 1.43 (m, 2H), 2.06 (br d, 2H), 2.36 (m, 3H), 2.52 (m, 1H), 2.82 (m, 2H), 3.07 (sex, 1H, J=7.2 Hz), 3.24 (m, 1H), 6.36 (t, 1H, J=75 Hz), 6.54 (d, 2H, J=9.0 Hz), 6.95 (d, 2H, J=9.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498346B2
Source datasetuspto-grants-2009_03
ORD IDord-b8ae91da14864fe0bf8de2cacaeb0d4d
Source noteuspto-grants-2009_03