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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248115Generated: October 30, 2026

Dimethylformamide → HCID 53752137, compound

https://huagongshe.com/reaction/2248115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 73656243HCID 73656243—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 53752137HCID 5375213763%

Reaction Steps

To a stirred solution of 3.22 g of 1,2,3,4,5,6-hexahydro-6,12-dimethyl-2,6-methano-9H-pyrrolo[3,2-h][3]benzazocine and 58 ml of dimethylformamide was added 4.70 ml of diisopropylethyl amine and then 1.56 ml of cyclopropylmethyl bromide, under nitrogen. The reaction mixture was warmed in an oil bath at 70°-80° C. for 1.5 hr and stirred at room temperature overnight. The reaction mixture was poured into water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate and ether. The combined organic layers were washed with brine, dried over anhydrous potassium carbonate, filtered, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, 2% triethylamine/0-10% methanol/ethyl acetate) gave 2.48 g (63%) of product. Sublimation (173°-175° C., ~0.3 mm) gave the analytical sample, mp 187°-190° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037985
Source datasetuspto-grants-1991_08
ORD IDord-68641b54d7ff418eb0580fd066a82420
Source noteuspto-grants-1991_08