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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885742Generated: November 3, 2026

Dimethylformamide → HCID 67897260, compound

https://huagongshe.com/reaction/1885742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 73656241HCID 73656241—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 67897260HCID 6789726023%

Reaction Steps

To a stirred solution of 0.99 g of 6,12-dimethyl-1,2,3,4,5,6-hexahydro-2,6-methano-8H-pyrrolo[2,3-i][3]benzazocine and 18 ml of dimethylformamide was added 1.44 ml of diisopropylethyl amine. Cyclopropylmethyl bromide (0.48 ml) was added, under nitrogen, and the reaction mixture was heated at 82°-83° C. for 6 hr. The reaction mixture was cooled to room temperature and was poured into ethyl acetate and water. The layers were separated and the aqueous layer extracted with ethyl acetate and ether. The combined organic layers were washed with water and brine, dried over anhydrous potassium carbonate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 2% triethylamine/0-15% methanol/ethyl acetate), a second column (silica gel, 2% triethylamine/ethyl acetate), and a third column (silica gel, 1% triethylamine/ether) to afford 0.28 g (23%) of the product, as an oil, which crystallized upon trituration with ether. Recrystallization from ether-pentane gave the analytical sample, mp 164°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145965
Source datasetuspto-grants-1992_09
ORD IDord-b2f65aeff4644f0fb07f328427c3b88d
Source noteuspto-grants-1992_09