HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902669Generated: November 1, 2026
Sodium Iodide → 8-[3-(Diphenylamino)propyl]-1-(4-methoxyphenyl)-1,3,8-triazaspiro[4,5]decan-4-one
https://huagongshe.com/reaction/1902669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-[N,N-diphenylamino)-1-bromopropane | HCID 10827329 | — |
| Reactant | 1-(4-Methoxyphenyl)-1,3,8-triazaspiro[4.5]decan-4-one | HCID 13240217 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 8-[3-(Diphenylamino)propyl]-1-(4-methoxyphenyl)-1,3,8-triazaspiro[4,5]decan-4-one | HCID 12763865 | — |
Reaction Steps
A mixture of 940 mg. (0.00325 moles) of 3-[N,N-diphenylamino)-1-bromopropane (prepared according to the procedure of Example 2) and 850 mg. (0.00325 moles) of 1-(4-methoxyphenyl)-1,3,8-triazaspiro[4,5]decan-4-one, 400 mg. of sodium carbonate and 100 mg. of sodium iodide in 15 ml. of methyl ethyl ketone is refluxed for about 16 hours. The preparation of 1-(4-methoxyphenyl)-1,3,8-triazaspiro[4,5]decan-4-one is described in United States Pat. No. 3,155,670 to Janssen, issued Nov. 3, 1964. Solvent is evaporated and the residue is dissolved in chloroform, washed with water and chromatographed on a column of silica gel. The product fractions are evaporated and the residue is recrystallized from isopropyl alcohol and again from ethanol, giving 470 mg. of 8-[3-diphenylamino)propyl]-1-(4-methoxyphenyl)-1,3,8-triazaspiro[4,5]decan-4-one, mp. 156.5°-157.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04364954 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-ca2dfeacb2ab464aab1eef43514fba43 |
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| Source note | uspto-grants-1982_12 |
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