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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460696Generated: November 1, 2026

Toluene → HCID 15725739, compound

https://huagongshe.com/reaction/1460696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 15725738HCID 15725738—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
ProductHCID 15725739HCID 1572573995.3%

Reaction Steps

A mixture of 3,4,5-triphenyl-1H-pyrazol-1-hexanol (5 g, 12 mmol), tert-butyl bromoacetate (4.92 g, 4.10 mL, 25 mmol), tetrabutylammonium hydrogen sulfate (0.4 g), 50% aqueous sodium hydroxide solution (80 mL) and toluene (80 mL) was stirred vigorously at room temperature. After I8 hours, the reaction mixture was diluted with water (100 mL), the organic layer separated and the aqueous layer extracted twice with diethyl ether. The combined extracts were dried over sodium sulfate and the solvent evaporated to give an oil which was chromatographed on a column of silica gel. Elution with a mixture of hexane and diethyl ether (2:1) afforded 1,1-dimethylethyl [[6-(3,4,5-triphenyl-1H-pyrazol-1-yl)hexyl]oxy]-acetate (5.84 g, 95%) as an oil that slowly crystallized to a white solid; m.p.=69°-72° C. MS(CI): m/e=511 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071866
Source datasetuspto-grants-1991_12
ORD IDord-1c95efb870474cfcad9b8eccb12efe35
Source noteuspto-grants-1991_12