HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 392486Erstellt: 24. Oktober 2026
Methylhydrazine → 2,5-dimethoxythiobenzoic acid N-methylhydrazide
https://huagongshe.com/de/reaction/392486
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylhydrazine | HCID 6061 | — |
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 2,5-Dimethoxybenzoic acid | HCID 76027 | — |
| Edukt | Lawesson's reagent | HCID 87949 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2,5-dimethoxythiobenzoic acid N-methylhydrazide | HCID 11333617 | 116,8% |
Reaktionsschritte
DCC (4.5 g, 21.8 mmol) was added in one portion to a solution of 2,5-dimethoxybenzoic acid (3.6 g, 20 mol), methylhydrazine (1.2 ml, 23 mmol) and DMAP (30 mg, cat.) in CH2Cl2 (60 ml) cooled in an ice bath. The reaction mixture was stirred overnight at room temperature. The slurry was cooled at −20° C. for 1 h and filtered. The CH2Cl2 solution was evaporated and the residue was dried in vacuum. The resulting crude product was dissolved in toluene (50 ml). To this solution was added Lawesson's reagent (5.8 g, 14 mmol). The mixture was refluxed for 40 min, cooled to room temperature, and directly subjected to silica gel column chromatography (eluent: 25% to 35% ethyl acetate in hexanes) to give the 2,5-dimethoxythiobenzoic acid N-methylhydrazide (3.7 g, yield: 82%) as off-white solid. 1H NMR (300 MHz, CDCl3): δ 6.88-6.80(m, 3H), 5.46 (s, 2H), 3.84(s, 3H), 3.82 (s, 3H), 3.28(s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06800660B2 |
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| Quelldatensatz | uspto-grants-2004_10 |
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| ORD ID | ord-dccdbabcbe5645f88a268f092bddaa97 |
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| Quellennotiz | uspto-grants-2004_10 |
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