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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261320Generated: October 26, 2026

2,5-Dimethoxytetrahydrofuran → ethyl 5-(1H-pyrrol-1-yl)-1-t-butyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/2261320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
Reactantethyl 5-amino-1-(tert-butyl)-1H-pyrazole-4-carboxylateHCID 13809946—
SolventAcetic AcidHCID 176—
Productethyl 5-(1H-pyrrol-1-yl)-1-t-butyl-1H-pyrazole-4-carboxylateHCID 5773636685.6%

Reaction Steps

8.45 g of ethyl 5-amino-1-t-butyl-1H-pyrazole-4-carboxylate was dissolved in 60 ml of acetic acid, and 7.93 g of 2,5-dimethoxytetrahydrofuran was then added. The mixture was heated to reflux for 2 hours. The reaction mixture was concentrated under reduced pressure. After water was added, the residue was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 8.95 g of ethyl 5-(1H-pyrrol-1-yl)-1-t-butyl-1H-pyrazole-4-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-de6d3e431d434b55b9eb46e49ffbc617
Source noteuspto-grants-2010_12