HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409796Generated: October 29, 2026
Methyl bromoacetate → HCID 140590450, compound
https://huagongshe.com/reaction/2409796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 88590350 | HCID 88590350 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 140590450 | HCID 140590450 | 76.1% |
Reaction Steps
To a solution of (E)-N-(4-methoxy-2,6-dimethylphenyl)-2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzylidene)hydrazine-carbothioamide (250 mg, 0.462 mmol) in EtOH (5 mL) was added methyl bromoacetate (100 mg, 0.65 mmol), and the mixture was heated to 70° C. for 4 h. The mixture was allowed to cool to room temperature and diluted with water (1 mL). The precipitate was vacuum filtered, giving the title compound as a white solid (204 mg, 76%): mp 188-190° C.; 1H NMR (400 MHz, CDCl3) δ 8.56 (s, 1H), 8.33 (s, 1H), 8.22 (d, J=8.1 Hz, 2H), 7.90-7.70 (m, 4H), 7.39 (d, J=8.7 Hz, 2H), 6.72 (s, 2H), 4.01 (s, 2H), 3.87-3.73 (s, 3H), 2.18 (s, 6H); ESIMS m/z 581 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815922B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-35029bdb86fa43db9f1b43085a474b7e |
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| Source note | uspto-grants-2014_08 |
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