Ammonia → 3-(Aminomethyl)-1,3-dihydro-2,1-benzoxaborol-1-ol hydrochloride

HRID 339611Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 339611
[N+:1]([CH2:4][CH:5]1[O:9][B:8]([OH:10])[C:7]2[CH:11]=[CH:12][CH:13]=[CH:14][C:6]1=2)([O-])=O.N.[ClH:16]>C(O)C.O.[Ni]>[ClH:16].[NH2:1][CH2:4][CH:5]1[O:9][B:8]([OH:10])[C:7]2[CH:11]=[CH:12][CH:13]=[CH:14][C:6]1=2

Komponenten

7

Versuchsvorschrift

To a solution of 3-(nitromethyl)benzo[c][1,2]oxaborol-1(3H)-ol (965 mg, 5 mmol) in ethanol (30 mL) were added ammonia (2M solution in ethanol, 18 mL, 36 mmol) and Raney 2800 Nickel (⅓ teaspoon of a slurry in water). The reaction mixture was subjected to hydrogenation at 45 atmospheres for 2 h at rt. The resulting mixture was filtered through Celite and the filtrate was concentrated in vacuo yielding the crude amine. The amine was dissolved in dioxanes (10 mL) and HCl (4M in dioxanes, 5 mL, 20 mmol) was added. After 1 h, the suspension was concentrated and the resulting solid was washed with hexanes followed by ether yielding 3-(aminomethyl)benzo[c][1,2]oxaborol-1(3H)-ol hydrochloride (917 mg, 4.6 mmol, 92% yield) as a white solid.

Aufarbeitung

  1. filtrationThe resulting mixture was filtered through Celite
  2. concentrationthe filtrate was concentrated in vacuo
  3. customyielding the crude amine
  4. waitAfter 1 h
  5. concentrationthe suspension was concentrated
  6. washthe resulting solid was washed with hexanes

Quellen und Nachweise

ORD-Eintrag
ord-9a38a27297b144ddbbce2559eadbe7d5
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08895534B2

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