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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471933Generated: October 29, 2026

Methanol → 2-(4-Phenyl-3-p-tolyl-1H-pyrazol-5-yl)ethanol

https://huagongshe.com/reaction/1471933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Allyl-4-phenyl-3-p-tolyl-1H-pyrazoleHCID 67384566—
Product2-(4-Phenyl-3-p-tolyl-1H-pyrazol-5-yl)ethanolHCID 67385029—

Reaction Steps

5-Allyl-4-phenyl-3-p-tolyl-1H-pyrazole (1.0 g, 3.64 mmol) was dissolved in methanol (40 mL) and dichloromethane (10 mL) and cooled to −78° C. on a dry-ice/acetone bath. Ozone was bubbled through the solution for h, until the solution appeared light blue. To the reaction was added sodium borohydride (0.138 g, 3.64 mmol) and the reaction was removed from the dry-ice bath and stirred at room temperature for 1 h. Excess solvent was removed under reduced pressure and the reaction was extracted with EtOAc/H2O, dried over MgSO4, and purified by column chromatography to give the title compound as white solid (0.54 g). LCMS m/z=279.2 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 2.25 (s, 3H), 2.71 (t, J=7.33 Hz, 2H), 3.57 (t, J=7.33 Hz, 2H), 4.65 (bs, 1H), 7.03-7.09 (m, 2H), 7.16-7.23 (m, 3H), 7.24-7.31 (m, 2H), 7.32-7.40 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012478B2
Source datasetuspto-grants-2015_04
ORD IDord-68c95bb6ada64975a2bbe4bdf90fee40
Source noteuspto-grants-2015_04