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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396848Generated: November 3, 2026

Trifluoroacetic acid → tert-butyl 4,5-dihydro-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1396848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl acrylateHCID 15458—
ReactantTrimethylsilyldiazomethaneHCID 167693—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4,5-dihydro-1H-pyrazole-5-carboxylateHCID 8670633841.1%

Reaction Steps

To a solution of t-butyl acrylate (17 g, 133 mmol) dissolved in toluene (200 mL) and n-hexanes (200 mL) was added TMS-diazomethane (99 mL, 199 mmol) over 10 minutes. After 1 h the reaction mixture was concentrated and the residue diluted with DCM (300 mL) and TFA (20.44 mL, 265 mmol) was added slowly over 15 minutes. After 30 minutes the reaction mixture was concentrated, basified with 1N NaOH and extracted into DCM (400 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, concentrated, and purified by filtration through a pad of silica gel eluting the product with 50% ethyl acetate/hexanes to afford 10 g (54.6 mmol) of 1,1-dimethylethyl 4,5-dihydro-1H-pyrazole-5-carboxylate as a yellow oil. LC-MS (ES) m/e 170.91 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-04d1c429c73e47e58e9c536121bef4ce
Source noteuspto-grants-2014_12