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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404136Generated: October 29, 2026

Triphenylphosphine → HCID 178445771, compound

https://huagongshe.com/reaction/2404136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant6-Hydroxy-2-naphthonitrileHCID 4589476—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 178445811HCID 178445811—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178445771HCID 178445771146.4%

Reaction Steps

To a vial charged with 6-hydroxy-2-naphthonitrile (3.38 g, 0.02 mol, 1.0 eq.), cis-4-tert-butylcyclohexanol (6.24 g, 0.04 mol, 2.0 eq.), PPh3 (10.5 g, 0.04 mol, 2.0 eq.) and toluene (20 mL), was added DIAD (12 mL, 0.06 mol, 3.0 eq.) under nitrogen atmosphere at r.t. and stirred for 15 h. Water was added and extracted with EtOAc. The organic layer was purified by silica gel chromatography (PE:EA=10:1) to give the title compound (9.0 g, 86%) as a slight yellow solid. EDI-MS (M+1)+: 308.0. 1H NMR (400 MHz, CDCl3) δ 8.12 (s, 1H), 7.78-7.73 (m, 2H), 7.54 (dd, 1H), 7.22 (dd, 1H), 7.14 (s, 1H), 4.33-4.30 (m, 1H), 2.29-2.25 (m, 2H), 1.93-1.90 (m, 2H), 1.48-1.26 (m, 2H), 1.25-1.10 (m, 3H), 0.91 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802659B2
Source datasetuspto-grants-2014_08
ORD IDord-c00fd199fa7d4b64b461b7feb25514ea
Source noteuspto-grants-2014_08