HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36722Erstellt: 25. Oktober 2026
Hydrochloric Acid → 4-(4-Chlorobenzyl)aniline
https://huagongshe.com/reaction/36722
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 4-Amino-4'-chlorobenzophenone | HCID 3528706 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-(4-Chlorobenzyl)aniline | HCID 282855 | 75,6% |
Reaktionsschritte
A suspension of 4.27 g (18.4 mmols) of 4-amino-4' chloro-benzophenone and 8.54 g of zinc amalgam in 80 ml of toluene containing 4 ml of water was heated to reflux. 1 ml of concentrated hydrochloric acid were added over 90 minutes. After 22 hours, the mixture was allowed to cool to room temperature and 100 ml of ethyl acetate and 2×100 ml of water were added. The layers were separated and the aqueous phase was extracted with 50 ml of ethyl acetate. The combined organics were washed twice with 100 ml of water and 50 ml of brine, dried over MgSO4, filtered and evaporated to obtain 3.03 g of orange oil. Flash chromatography (20-35% ethyl acetate/pet ether eluent) yielded the above mentioned product as an orange liquid 915 mg (24.6% yield). 1H nmr (CDCl3) δ3.58 (2H, br s) , 3.82 (2H, s), 6.62 (2H, d), 6.94 (2H, d), 7.08 (2H, d), 7.22 (2H, d)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05416112 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-3fb56c4328cf4a9186492b7af4000546 |
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| Quellennotiz | uspto-grants-1995_05 |
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