HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092670Generated: November 2, 2026
N,N'-Dimethylethylenediamine → HCID 66579660, compound
https://huagongshe.com/reaction/2092670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 53829389 | HCID 53829389 | — |
| Reactant | 1,4-Dioxa-10-azadispiro[4.2.4.2]tetradecan-9-one | HCID 58230108 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66579660 | HCID 66579660 | — |
Reaction Steps
1,4-Dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-one (276 mg, obtained in example 121, step 3) was dissolved in DMF (18 mL) at r.t. Then, 1-bromo-4-(3-methoxy-propyl)-benzene (599 mg, obtained in example 130, step 2), N,N′-dimethylethylenediamine (sym) (230 mg), Cuprous iodide (373 mg) and K3PO4 (832 mg) were added to the reaction mixture and the mixture was heated to 80° C. for 3 hours. The reaction mixture was cooled, poured into ice/water and was extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The title compound was obtained as a yellow liquid (460 mg, 93%) and was used without further purification. MS (m/e): 360.2. [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440710B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-d3203ce06d50432494f5ff56d36e8294 |
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| Source note | uspto-grants-2013_05 |
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