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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961603Generated: October 26, 2026

Iodocyclopentane → 5-Cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/reaction/1961603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodocyclopentaneHCID 73784—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68626191—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862582742%

Reaction Steps

5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12a was dissolved in 30 mL of N,N-dimethylformamide followed by addition of iodo-cyclopentane (5.4 g, 27.5 mmol) and lithium hexamethyldisilazide (27.5 mL, 27.5 mmol) under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was diluted with 10 mL of water and concentrated to remove N,N-dimethylformamide and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 5-cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 16a (2.6 g, yield 42%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415349B2
Source datasetuspto-grants-2013_04
ORD IDord-c4db9e08703f41afbb514a26c29d97cc
Source noteuspto-grants-2013_04