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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904175Generated: October 26, 2026

Triethylamine → (6-Cyanohexyl)bis(2-phthalimidoethyl)amine

https://huagongshe.com/reaction/1904175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHeptanenitrile, 7-bromo-HCID 88737—
Reactant2,2'-[iminobis(ethane-2,1-diyl)]bis(1H-isoindole-1,3(2H)-dione)HCID 354707—
SolventDimethylformamideHCID 6228—
Product(6-Cyanohexyl)bis(2-phthalimidoethyl)amineHCID 1981107841%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-bromohexylcyanide (13.88g, 0.073 mol), bis(2-phthalimidoethyl)amine (26.52g, 0.073 mol), and triethylamine (7.37g, 0.073 mol) in DMF (120 ml) was heated at 100° C. for 20 hours. After cooling, the precipitate which had formed was removed by filtration and the filtrate was poured into ice (1000 ml). The aqueous solution was extracted with dichloromethane (3×200 ml). The combined organic extracts were washed with brine and dried over Na2SO4. Removal of the solvent under reduced pressure gave crude product which was chromatographed on silica gel (hexanes - 30% ethyl acetate/hexanes gradient elution). Impure fractions were rechromatographed to provide a total of 14.1g of (6-cyanohexyl)bis(2-phthalimidoethyl)amine (41%) as an oil. The produce was one spot on tlc. The ir spectrum was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837003
Source datasetuspto-grants-1989_06
ORD IDord-483dd1139f19449084535fe7a6099335
Source noteuspto-grants-1989_06