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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475503Generated: October 29, 2026

Benzyl Bromide → 2-Benzyl-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide

https://huagongshe.com/reaction/475503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
Reactant1H,4H,5H,6H-cyclopenta[c]pyrazole-3-carboxamideHCID 45121258—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amideHCID 58713629—
Product2-Benzyl-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amideHCID 69304477196.4%

Reaction Steps

To a solution of 1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide (41.5 g, 275 mmol) in THF (460 mL) at rt was added a solution of NaOH (5N aq., 110 mL, 0.54 mol). After stirring for 5 min benzyl bromide (49.2 g, 0.29 mol) was added and the reaction was stirred for 16 h. The volatiles were removed in vacuo and the resulting solid was washed with H2O (3×250 mL). Further concentration gave regioisomers of 1-benzyl-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide and 2-benzyl-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid amide (65.3 g, 270 mmol, 98% yield) as a 20:1 mixture and was used without separation).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637555B2
Source datasetuspto-grants-2014_01
ORD IDord-82cb83c953dc4b479df7343cf5e60f7f
Source noteuspto-grants-2014_01