HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509693Generated: October 29, 2026
Phenethyl bromide → 1-(4-Methylphenyl)-1-(2-phenylethyl)hydrazine
https://huagongshe.com/reaction/509693
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylphenylhydrazine monohydrochloride | HCID 12504 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Methylphenyl)-1-(2-phenylethyl)hydrazine | HCID 57876021 | 26% |
Reaction Steps
p-Tolylhydrazine hydrochloride (10.0 g, 63 mmol) was suspended in EtOH (45 mL). To this suspension was added triethylamine (9.0 mL, 63 mmol) drop-wise over a period of 5-10 minutes. The reaction mixture was stirred for additional 10 minutes. Phenethyl bromide (9 mL, 63 mmol) was added drop-wise at 25° C. over a period of 10 to 15 minutes. The reaction mixture was heated at 80° C. for 2 h at which point the reaction was found complete by TLC and LC-MS. The reaction mixture was concentrated under reduced pressure, the residue was suspended in saturated aqueous NaHCO3 (pH 9) and extracted with ethyl acetate (100 mL×2). The organic layer was separated, dried (Na2SO4) and concentrated to obtain crude product as a dark brown oil (14 g). Purification of crude product by flash column chromatography (silica gel, 230-400 mesh, eluent: 8-10% ethyl acetate-hexanes) furnished 3.7 g of pure product as yellow oil. Yield: 26% (unoptimized).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096591B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-35e42e77d6bf464eb840ac8d40b5ddee |
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| Source note | uspto-grants-2015_08 |
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