HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505947Generated: November 3, 2026
N,N,N',N'-Tetramethylethylenediamine → 4-Phenylpentan-2-ylbenzene
https://huagongshe.com/reaction/505947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 2,4-Dichloropentane | HCID 12261 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Phenylpentan-2-ylbenzene | HCID 244014 | — |
Reaction Steps
A mixture of phenyl magnesium bromide (1.25 mL of 0.96 M THF solution, 1.2 mmol) and TMEDA (181.1 μL, 1.2 mmol) was added to a solution of 2,4-dichloropentane (70.5 mg, 0.5 mmol) and FeCl3 (0.5 mL of 0.1 M THF solution, 0.05 mmol) in THF (0.5 mL) at 50° C. over an hour through a syringe pump. The resulting mixture was stirred at the temperature for 20 minutes and saturated ammonium chloride aqueous solution was added thereto to terminate the reaction, followed by diluting with 3 mL of ethyl acetate. The dilution was filtered through a packed silica gel (eluent: ethyl acetate) followed by concentration under reduced pressure. 1H NMR analysis indicates that the desired product was obtained in almost quantitative yield. Purification by recycling GPC gave the pure compound in a yield of 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781599B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-ddfcef9722f9420fb90054b2f89f33f2 |
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| Source note | uspto-grants-2010_08 |
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