HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703751Generated: October 29, 2026
1-Bromooctadecane → 15-Octadecyl-7,15-diazadispiro[5.1.5~8~.3~6~]hexadecane-14,16-dione
https://huagongshe.com/reaction/1703751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctadecane | HCID 8218 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7,15-Diazadispiro[5.1.5.3]hexadecane-14,16-dione | HCID 12234739 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 15-Octadecyl-7,15-diazadispiro[5.1.5~8~.3~6~]hexadecane-14,16-dione | HCID 18533676 | — |
Reaction Steps
To a solution of 10.0 g (0.04 moles) of 7,15-diazadispiro [5,1,5,3] hexadecane-14,16-dione in 150 ml of anhydrous methanol in a 500 ml flask was added 2.6 g. of 86% KOH (0.04 moles) and the mixture was shaken until solution was obtained. The reaction mixture was then evaporated to dryness under reduced pressure. The residue was transferred to a 300 ml 3-necked flask equipped with a stirrer, thermometer, condenser with drying tube, dropping funnel and nitrogen inlet with the aid of a small amount of dry DMF. To the potassium imide salt, under a nitrogen atmosphere, was added 150 ml of dry DMF. To the stirred solution was added dropwise a solution of 13.3 g. (0.04 moles) of n-octadecyl bromide in 50 ml of DMF. The reaction mixture was heated slowly to 75° C. and held at that temperature for 3 hours. The reaction mixture was cooled and allowed to stand at room temperature overnight. The reaction mixture was then taken up in 500 ml ether, the ether solution washed well with water, dried over anhydrous Na2SO4 and evaporated under reduced pressure. The residue, which crystallized on standing, was recrystallized from methanol yielding 14.3 g of white needles as the product, m.p. 39°-40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125517 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-0b9f4701a21d4a2f92c253cd1076e7ee |
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| Source note | uspto-grants-1978_11 |
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