Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961579Generated: October 31, 2026

Sodium Carbonate → 5-Isocyano-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/reaction/1961579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant5-Methylene-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68625478—
CatalystSilver perchlorateHCID 24562—
SolventDichloromethaneHCID 6344—
Product5-Isocyano-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 7233893318.1%

Reaction Steps

5-Methylene-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 11a (1.6 g, 8.23 mmol) was dissolved in 30 mL of dichloromethane with stirring followed by addition of trimethylsilyl cyanide (4.08 g, 41.2 mmol) and silver perchlorate (5.12 g, 24.7 mmol) under nitrogen atmosphere. The reaction mixture was stirred overnight at room temperature and then some of the reaction mixture was treated with saturated aqueous sodium carbonate. The reaction was monitored by TLC, which showed that there remained most of the starting materials. Then the mixture was treated with 20 mL of saturated aqueous sodium carbonate upon cooling by an ice-water bath, and the reaction released heat. After 10 minutes, the mixture was filtered to remove the residue. The separated aqueous phase was extracted with ethyl acetate (50 mL×4). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 5-isocyano-5-methyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 11b (0.33 g, yield 18.1%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415349B2
Source datasetuspto-grants-2013_04
ORD IDord-bc5e30250b0e49d28694ffabba5d2bf1
Source noteuspto-grants-2013_04