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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420978Generated: November 3, 2026

Triphenylphosphine → HCID 57434763, compound

https://huagongshe.com/reaction/2420978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-CyanophenolHCID 13394—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant4-(1-Methyl-piperidin-4-yl)-butan-1-olHCID 23033965—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57434763HCID 5743476371%

Reaction Steps

To a 0° C. solution of 4-(1-methyl-piperidin-4-yl)-butan-1-ol (0.74 g, 4.37 mmol), 3-hydroxy-benzonitrile (0.52 g, 4.37 mmol), and 3 mmol/g polymer supported PPh3 (2.30 g, 8.73 mmol) in THF (40 mL) was added diisopropyl azodicarboxylate (1.72 mL, 8.73 mmol) dropwise. After 6 h the mixture was filtered and concentrated. Purification by Method 1 afforded 840 mg (71%) of a yellow oil. MS (ESI): mass calcd for C17H24N2O, 272.19; m/z found, 273.4 [M+H]+. 1H NMR (400 MHz, CDCl3): 7.38-7.33 (m, 1H), 7.24-7.20 (m, 1H), 7.14-7.09 (m, 2H), 3.96 (t, J=6.4, 2H), 2.88-2.80 (m, 2H), 2.26 (s, 3H), 1.94-1.84 (m, 2H), 1.82-1.73 (m, 2H), 1.72-1.64 (m, 2H), 1.52-1.42 (m, 2H), 1.34-1.17 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956066B2
Source datasetuspto-grants-2011_06
ORD IDord-d51469fd9d3c4bdf8c6b8d77fd304d21
Source noteuspto-grants-2011_06