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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | 1-Heptanamine | HCID 8127 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-[4-(Heptylamino)butyl]azepan-2-one | HCID 14625930 | 70.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04882359 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-ac02bf17223642fb8bde916fac411a1a |
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| Source note | uspto-grants-1989_11 |
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