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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185175Generated: October 31, 2026

Thionyl Chloride → Ethyl 2-(5-(Chloromethyl)-3-nitro-1H-pyrazol-1-yl)acetate

https://huagongshe.com/reaction/1185175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 2-(5-(Hydroxymethyl)-3-nitro-1H-pyrazol-1-yl)acetateHCID 86684029—
SolventChloroformHCID 6212—
ProductEthyl 2-(5-(Chloromethyl)-3-nitro-1H-pyrazol-1-yl)acetateHCID 8668403068%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 146a (1.50 g, 6.55 mmol) in CHCl3 (60 mL) cooled at 0° C. was slowly added SOCl2 (2.34 g, 19.6 mmol) while maintaining the internal temperature below 5° C. This reaction mixture was warmed to 50° C. and stirred at this temperature for 3 h. It was then cooled to 0° C. and quenched with water. The organic layer was separated and evaporated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with 30:1 dichloromethane/methanol to afford 146b (1.1 g, 68%) as a yellow solid. MS-ESI: [M+H]+ 247.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669251B2
Source datasetuspto-grants-2014_03
ORD IDord-fd776d5652e343b39d52620162e95ca4
Source noteuspto-grants-2014_03