HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376840Generated: October 30, 2026
Methylhydrazine → HCID 19360031, compound
https://huagongshe.com/reaction/376840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenamine, 2-phenoxy- | HCID 75899 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 19360031 | HCID 19360031 | 50% |
Reaction Steps
2-Phenoxyaniline (5.57 g) and triethylamine (4.2 mL) were dissolved in 100 mL of 1,2-dichloroethane. Triphosgene (Cl3COC(=O)OCCl3, 2.97 g) was added and a precipitate formed. The mixture was heated to reflux and the solid redissolved. After 5.5 h, the solution was cooled and 1.6 mL of methyl hydrazine was added and a new precipitate formed. The mixture was stirred at room temperature overnight. The solvent was removed and the residue was partitioned between ethyl acetate and 1N aqueous HCl solution. The organic phases were dried (MgSO4), filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography (1:1 hexane:ethyl acetate as eluant). The second-least polar component was collected, the eluant was removed under reduced pressure, and the residue was triturated with hexane to afford 3.86 g (50%) of the title compound of Step A, m.p. 117-119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022870 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-c23b8221ef1a4be5a750d04e72ad9f10 |
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| Source note | uspto-grants-2000_02 |
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