HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917088Generated: October 31, 2026
Triphenylphosphine → 6-bromo-4-methyl-2-(2-thiophen-2-yl-ethyl)-2H-[1,2,4]triazine-3,5-dione
https://huagongshe.com/reaction/1917088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Thiopheneethanol | HCID 79400 | — |
| Reactant | 6-bromo-4-methyl-1,2,4-triazine-3,5(2h,4h)-dione | HCID 260564 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-bromo-4-methyl-2-(2-thiophen-2-yl-ethyl)-2H-[1,2,4]triazine-3,5-dione | HCID 58269803 | 79% |
Reaction Steps
0.4 g (1.94 mmol) of intermediate 2a are placed in the presence of 0.24 mL (2.14 mmol) of 2-thiophen-2-yl-ethanol, 0.61 g (2.33 mmol) of triphenylphosphine in 4 mL of THF. At 0° C., 0.54 mL (2.33 mmol) of DEAD in solution in toluene are added dropwise. The reaction medium is heated for 7 h at 70° C. After concentration, the obtained residue is taken up with ethyl acetate and washed with water. After drying on MgSO4, the organic phase is dry concentrated. The obtained residue is purified by flash chromatography on silica (CH2Cl2/MeOH, gradient 100/0 to 97/3 over 30 min). 0.48 g of crystals corresponding to the compound 4k are obtained (yield: 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618287B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-d8930fc73b854711bb04d529f1351cbd |
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| Source note | uspto-grants-2013_12 |
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