HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21378Erstellt: 23. Oktober 2026
N-butyl-4-chlorobenzamide → n-Butyl-4-chlorobenzenemethanamine
https://huagongshe.com/de/reaction/21378
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-butyl-4-chlorobenzamide | HCID 346664 | — |
| Edukt | Hydrate;hydrochloride | HCID 21885828 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | n-Butyl-4-chlorobenzenemethanamine | HCID 57375995 | 164,6% |
Reaktionsschritte
A solution of N-butyl-4-chlorobenzamide (2.26 g; 0.011 mol) in dry THF (25 ml) was added slowly to an ice-cooled solution of 1.0M B2H6 --THF complex (45 ml; 0.045 tool) under a nitrogen blanket. When addition was complete, the mixture was stirred and heated to reflux for 3 hours, cooled and decomposed by dropwise addition of 1:1 conc aq HCl-water (10 ml). The mixture was then evaporated on a rotary evaporator at 60° for 1/2 hour to decompose the boron-amine complexes. The residue was taken up in water, strongly basified with aq NaOH and extracted with CH2Cl2 (3×25 ml). The combined extracts were washed with water, dried (MgSO4), filtered and evaporated to give n-butyl-4-chlorobenzenemethanamine (1.79 g) as an oil. The oil was converted to the hydrochloride salt of the title compound (1.98 g) by crystallising from ethanolic HCl and ethyl acetate, mp 250°-252° after melting and resolidifying at 203°-207° .
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05422355 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-78f7e330337c40a8bdfa74f1db69078a |
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| Quellennotiz | uspto-grants-1995_06 |
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