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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698222Generated: November 2, 2026

1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehyde → 1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-ol

https://huagongshe.com/reaction/1698222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehydeHCID 59278370—
ReactantHCID 178461633HCID 178461633—
SolventTetrahydrofuranHCID 8028—
SolventAmmonia chlorideHCID 20976574—
Product1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-olHCID 59278348—

Reaction Steps

To a chilled (−40° C.) solution of 1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehyde (1.50 g, 5.99 mmol) in THF was added a 2 M solution of ethylmagnesium chloride (3.00 mL, 6.00 mmol) in THF. After 3 hours, the mixture was diluted with saturated aqueous ammonia chloride and extracted with EtOAc. The combined organic layers were washed with brine, dried over sodium sulfate and the concentrated in vacuo. The residue was purified by reversed-phase HPLC. The major fractions were combined and the solvent was concentrated in vacuo to afford 1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163918B2
Source datasetuspto-grants-2012_04
ORD IDord-b22d0ac40ed14dbb8b3ead96c8f63a0c
Source noteuspto-grants-2012_04