Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436321Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 12894308, compound

https://huagongshe.com/reaction/436321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant3-(Dimethylamino)propyl chloride hydrochlorideHCID 94308—
ReactantHCID 12369109HCID 12369109—
SolventWaterHCID 962—
ProductHCID 12894308HCID 1289430840.4%

Reaction Conditions

Temperature15 °C

Reaction Steps

To a solution prepared by heating 23.2 g. (0.55 mole) of a 67% mineral oil dispersion of sodium hydride in 200 ml. of anhydrous dimethylsulfoxide was added 50.5 g. (0.25 mole) of the 2,4,5,6-tetrahydro-1,3,4,6,6-pentamethylcyclopenta[c]pyrrole-4-carbonitrile described above in Example 3. The mixture was stirred under nitrogen for about two hours, cooled to 15° C., and treated with 39.5 g. (0.25 mole) of 3-chloro-N,N-dimethylpropylamine hydrochloride. When the foaming had subsided, the mixture was stirred at room temperature overnight, poured into water, and the gummy solid which separated was taken into diethyl ether and the solution washed first with water, then with saturated brine, dried and taken to dryness to give 69 g. of a solid which was recrystallized once from hexane and once from isopropanol to give 29 g of 2-[3-(di-methylamino)propyl]-2,4,5,6-tetrahydro-1,3,4,6,6-pentamethylcyclopenta[c]pyrrole-4-carbonitrile, m.p. 90.5°-91.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04008250
Source datasetuspto-grants-1977_02
ORD IDord-178efedd958d4bcd8e765f2552e4bad8
Source noteuspto-grants-1977_02