HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724930Generated: October 30, 2026
1-Ethenyl-3-methylbenzene → HCID 69945928, compound
https://huagongshe.com/reaction/724930
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethenyl-3-methylbenzene | HCID 7529 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10547779 | HCID 10547779 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69945928 | HCID 69945928 | 87.7% |
Reaction Steps
A mixture of 5,11-dihydro-11-ethyl-8-iodo-5-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (0.15 g, 0.4 mmol), 3-methylstyrene (0.05 mL, 0.4 mmol), palladium acetate (29 mg, 0.13 mmol), sodium bicarbonate (83 mg, 1.0 mmol), tetrabutylammonium chloride (0.11 g, 0.47 mmol), and 1 crystal of BHT in 2 mL of N,N-dimethylformamide was heated at 90° C. under argon for 4.5 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried (magnesium sulfate), and concentrated. Purification by flash chromatography, eluting with ethyl acetate/hexanes, afforded 0.13 g of the title compound, m.p. 207°-208° C. (ethyl acetate/hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05705499 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-0f3af44016464a439aa6424a5b78f39e |
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| Source note | uspto-grants-1998_01 |
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