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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381320Generated: November 2, 2026

o-Cyclohexylphenol → HCID 57919274, compound

https://huagongshe.com/reaction/2381320

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-CyclohexylphenolHCID 8396—
Reactant4,5-Dichloro-2-(tetrahydro-pyran-2-yl)-2H-pyridazin-3-oneHCID 10729262—
ReactantMethyl 2-bromo-3-cyclopentylpropanoateHCID 57919172—
ProductHCID 57919274HCID 5791927472%

Reaction Steps

In an analogous manner to the stepwise sequence outlined in intermediate 19, starting from 4,5-dichloro-2-(tetrahydropyran-2-yl)-2H-pyridazin-3-one (Intermediate 20) and 2-cyclohexylphenol and alkylating with 2-bromo-3-cyclopentyl-propionic acid methyl ester (Intermediate 10) afforded 2-[4-(2-cyclohexylphenoxy)-6-oxo-6H-pyridazin-1-yl]-3-cyclopentylpropionic acid (17.1 g, 72%) as a white solid; LC-MS [M+H+]=411.2; HPLC (0.17% trifluoroacetic acid in acetonitrile/water, 50%-100% acetonitrile, gradient, 1 mL/min, Venusil MP-C18, C18-15 cm×4.6 mm-5 μm), 254 nm, 95.8%, 214 nm, 97.2%. 1H-NMR (CDCl3, 300 MHz) δ 1.04-1.77 (m, 19H), 2.05-2.11 (m, 1H), 2.22-2.31 (m, 1H), 2.59-2.66 (t, 1H), 5.27-5.32 (dd, J=10.2 Hz, 4.8 Hz, 1H), 5.88-5.89 (d, J=2.4 Hz, 1H), 6.98-7.00 (m, 1H), 7.19-7.26 (m, 2H), 7.34-7.37 (m, 1H), 7.84-7.85 (d, J=2.7 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258134B2
Source datasetuspto-grants-2012_09
ORD IDord-785c7517495b4f4887a05074f6fcbbad
Source noteuspto-grants-2012_09