Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475501Generated: October 30, 2026

Benzyl Bromide → 2-Benzyl-2,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide

https://huagongshe.com/reaction/475501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1H,4H,5H,6H-cyclopenta[c]pyrazole-3-carboxamideHCID 45121258—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Benzyl-2,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amideHCID 5871364718.1%

Reaction Steps

To a stirring solution of 1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide (2.57 g, 17.0 mmol) in DMF (34 mL) at 25° C. was added K2CO3 (5.87 g, 42.5 mmol) followed by benzyl bromide (4.36 g g, 25.5 mmol). The reaction was stirred at ambient temperature for 16 h at which time the mixture was diluted with EtOAc (75 mL) and filtered. The filtrate was washed with H2O (100 mL) and the aqueous phase was back-extracted with EtOAc (75 mL) and CH2Cl2 (75 mL). The combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. Purification by silica gel chromatography (50% EtOAc in hexanes gradient to 95% EtOAc in hexanes) gave 2-benzyl-2,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide (739 mg, 3.07 mmol, 18% yield) isolated as a white solid followed by 1-benzyl-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide (3.24 g, 13.4 mmol, 79% yield) isolated as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637555B2
Source datasetuspto-grants-2014_01
ORD IDord-614abc68c85742719d31fd47f54b3dc9
Source noteuspto-grants-2014_01