HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 726310Erstellt: 24. Oktober 2026
Hydrazine hydrate (1:1) → 3-(Tert-butyldiphenylsilyloxymethyl)-2,4-dichloroaniline
https://huagongshe.com/de/reaction/726310
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | 1-(Tert-butyldiphenylsilyloxymethyl)-2,6-dichloro-3-nitrobenzene | HCID 11798185 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-(Tert-butyldiphenylsilyloxymethyl)-2,4-dichloroaniline | HCID 10598719 | 86% |
Reaktionsschritte
To a stirred mixture of 1-(tert-butyldiphenylsilyloxymethyl)-2,6-dichloro-3-nitrobenzene (433 mg), ferric chloride hexahydrate (17.5 mg) and activated carbon (17.5 mg) in a mixture of methanol (2.78 ml) and water (0.69 ml) was added hydrazine monohydrate (0.135 ml) dropwise at 60-70° C. After the addition was finished, the mixture was refluxed for half an hour. The mixture was allowed to cool and filtered. The filtrate was concentrated in vacuo. The residue was extracted with dichloromethane and the organic phase was dried over anhydrous magnesium sulfate. After being filtered, the filtrate was concentrated in vacuo and the resulting residue was washed with n-hexane to give 3-amino-1-(tert-butyldiphenylsilyloxymethyl)-2,6-dichlorobenzene (348 mg) as a white mass.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05708173 |
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| Quelldatensatz | uspto-grants-1998_01 |
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| ORD ID | ord-66d50a106bdf4ebea8f3dfbc9d525d92 |
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| Quellennotiz | uspto-grants-1998_01 |
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