Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041515Generated: November 3, 2026

Cycloheptanol → 4-(Cycloheptyloxy)benzonitrile

https://huagongshe.com/reaction/2041515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloheptanolHCID 10399—
Reactant4-CyanophenolHCID 13019—
ReactantTributylphosphineHCID 13831—
ReactantAzodicarboxylate dipiperidineHCID 66707187—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-(Cycloheptyloxy)benzonitrileHCID 5765662558%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, add 4-hydroxybenzonitrile (4 g, 33.5 mmol), cycloheptanol (2.55 g, 22.3 mmol), tri-n-butylphosphine (8.25 mL, 33.5 mmol), and azodicarboxylate dipiperidine (8.45 g, 33.5 mmol) to anhydrous THF (60 mL) at 0° C. Stir the mixture at 0° C. for 1 h and then at room temperature for 12 h. Dilute with EtOAc (50 mL) and water (50 mL). Separate the layers and extract the aqueous phase with EtOAc (4×30 mL). Wash the combined organic extracts with water (30 mL) and brine (20 mL). Dry over Na2SO4, filter and concentrate in vacuo. Purify the crude mixture by chromatography on silica gel (120 g RediSep column) eluting with hexane/EtOAc (1:0 to 1:1 gradient over 1.25 h; 80 mL/min) to provide the desired intermediate as a colorless oil (2.77 g, 58%). MS (APCI) m/z: 216 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-4ddab00f7e0a4270b51172d32f4795eb
Source noteuspto-grants-2013_11