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Hydroxyamine hydrochloride → 4-Carbazol-9-ylmethyl-N-hydroxybenzamide

HRID 403633
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 403633
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]2[C:23]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[C:17]3[C:12]2=[CH:13][CH:14]=[CH:15][CH:16]=3)=[CH:6][CH:5]=1.Cl.[NH2:26][OH:27].C[O-].[Na+]>CO.C(OCC)(=O)C.C(=O)(O)[O-].[Na+]>[CH:22]1[C:23]2[N:11]([CH2:10][C:7]3[CH:8]=[CH:9][C:4]([C:3]([NH:26][OH:27])=[O:2])=[CH:5][CH:6]=3)[C:12]3[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=3)[C:18]=2[CH:19]=[CH:20][CH:21]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 443297Hydroxyamine hydrochlorideHCID 10942334Sodium MethoxideHCID 668730724-Carbazol-9-ylmethylbenzoic acid methyl ester

Produkt 1

HCID 469188244-Carbazol-9-ylmethyl-N-hydroxybenzamideAusbeute 41 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittel2×
HCID 8857
Ethyl Acetate
Lösungsmittel
HCID 516892Sodium BicarbonateLösungsmittel

Versuchsvorschrift

4-Carbazol-9-ylmethylbenzoic acid methyl ester (19) (1.0 g, 3.2 mmol) and hydroxylamine hydrochloride (1.3 g, 19.0 mmol) were placed under argon and dissolved in 5 mL of methanol. To it was added a 25% sodium methoxide solution in methanol (5.48 g, 25.4 mmol) which resulted in the formation of a white precipitate. The reaction was stirred for 24 h at room temperature after which the reaction was diluted with 20 mL ethyl acetate and 20 mL of saturated sodium bicarbonate. The organic layer was isolated and the aqueous layer was further extracted with ethyl acetate (2×10 mL). The combined organic layers were washed with brine (10 mL), dried (Na2SO4) and concentrated in vacuo. The crude extract was purified by HPLC to yield the title compound (0.41 g, 41%) as an off-white solid. 1H NMR (400 MHz, DMSO): δ 11.09 (s, 1H), 8.97 (s, 1H), 8.18 (d, 2H, J=7.8 Hz), 7.61 (m, 4H), 7.43 (t, 2H, J=8.0 Hz), 7.19 (m, 4H), 5.71 (s, 2H). 13C NMR (100 MHz, DMSO): δ 164.0, 140.2, 141.1, 132.0, 127.3, 126.8, 126.0, 122.3, 120.5, 119.2, 109.5, 45.4. ESI-HRMS (m/z): [M+H]+ calcd. for C21H17NO2, 317.1149. found, 317.1143. Analytical HPLC: Purity=99%, tR=10.69 min, Method A.

Aufarbeitung

  1. customresulted in the formation of a white precipitate
  2. customThe organic layer was isolated
  3. extractionthe aqueous layer was further extracted with ethyl acetate (2×10 mL)
  4. washThe combined organic layers were washed with brine (10 mL)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. extractionThe crude extract
  8. customwas purified by HPLC

Quellen und Nachweise

ORD-Eintrag
ord-8dfa79801eda45d3ad71ab1778820a0e
Quelldatensatz
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08748451B2

Notizen zur Reaktion

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