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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639122Generated: November 2, 2026

Caprolactam → 1-[4-(Heptylamino)butyl]azepan-2-one

https://huagongshe.com/reaction/1639122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCaprolactamHCID 7768—
Reactant1,4-DibromobutaneHCID 8056—
Reactant1-HeptanamineHCID 8127—
ReactantSodium hydrideHCID 24758—
SolventBenzeneHCID 241—
SolventTolueneHCID 1140—
Product1-[4-(Heptylamino)butyl]azepan-2-oneHCID 1462593070.8%

Reaction Steps

A mixture of 0.88 g of 60% sodium hydride and 200 ml of dry toluene was incorporated dropwise with a solution of 2.26 g of azacycloheptane-2-one in toluene, heated under reflux for one hour, thereafter incorporated with 17.3 g of 1,4-dibromobutane, further refluxed for 18 hours and then filtered to remove insoluble materials to obtain a filtrate. The thus obtained filtrate was washed with water, dried, freed from the solvent by distillation off at reduced pressure and then finally distilled to obtain an oily substance. A mixture of 3.92 g of the thus obtained oily substance, 1.82 g of n-heptylamine and 50 ml of benzene was incorporated dropwise with 2.64 g of 1,8-diazabicyclo [5,4,0] undecene-7 (DBU) in benzene and agitated at room temperature for a whole day. The thus obtained reaction mixture (liquid state) was washed with water, dried, freed from the solvent by distillation off at reduced pressure and then finally distilled to obtain 3.16 g of colorless 1-[4-(n-heptylamino) butyl] azacycloheptane-2-one having the following appearance, column temperature and analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882359
Source datasetuspto-grants-1989_11
ORD IDord-ac02bf17223642fb8bde916fac411a1a
Source noteuspto-grants-1989_11