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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267056Generated: October 25, 2026

Triphenylphosphine → HCID 59599582, compound

https://huagongshe.com/reaction/2267056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-(2,4-Dihydroxy-3-methylphenyl)ethan-1-oneHCID 592139—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant5-(3-(Hydroxymethyl)phenylthio)nicotinonitrileHCID 68538069—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59599582HCID 5959958250.5%

Reaction Steps

Add triphenylphosphine (5.24 g, 20.0 mmol) and diisopropylazodicarboxylate (4.04 g, 20.0 mmol) to a solution of 5-(3-(hydroxymethyl)phenylthio)nicotinonitrile (4.84 g, 20.0 mmol) and 1-(2,4-dihydroxy-3-methylphenyl)ethanone (3.32 g, 20.0 mmol) in THF (100 mL). Stir the reaction for 24 h. Quench the reaction with water and extract with EtOAc. Dry, filter and concentrate. Purify the residue by flash chromatography on silica gel eluting with a mixture of EtOAc and hexanes (15:85 to 20:80) to give an off-white solid. Recrystallize the solid from a mixture of EtOAc and hexanes to afford the title compound (3.94 g, 50%): 1H NMR (CDCl3) δ 2.14 (s, 3H), 2.57 (s, 3H), 5.18 (s, 2H), 6.44 (d, J=9.0 Hz, 1H), 7.46-7.49 (m, 3H), 7.52 (s, 1H), 7.59 (d, J=9.0 Hz, 1H), 7.62-7.63 (m, 1H), 8.63-8.64 (m, 2H), 12.78 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858646B2
Source datasetuspto-grants-2010_12
ORD IDord-bcd7229c1bcf42b98d08a445d65c2a01
Source noteuspto-grants-2010_12