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Stannous Chloride → 2-Amino-5-(trifluoromethyl)phenol

HRID 323021
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 323021
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:5]=1[OH:14])([O-])=O.Cl[Sn]Cl>CCO>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:11])([F:12])[F:13])=[CH:6][C:5]=1[OH:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24479Stannous ChlorideHCID 140916902-Nitro-5-(trifluoromethyl)phenol

Produkt 1

HCID 155242772-Amino-5-(trifluoromethyl)phenol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

2-Amino-5-trifluoromethylphenol was prepared by treating 2-nitro-5-trifluoromethylphenol (500 mg, 2.41 mmol) with a solution of SnCl2(3.5 g, mmol) in EtOH at 23° C. for 12 h. The mixture was concentrated to 50 mL and adjusted to pH 7 using saturated sodium bicarbonate. The reaction mixture was partitioned between H2O and EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The resulting colorless oil (370 mg, 87%) was used without further purification. 1H NMR (CDCl3): 7.6 (s, 1H), 7.39 (d, 1H, J=8.5 Hz), 7.08 (d, 1H, J=8.5 Hz)

Aufarbeitung

  1. concentrationThe mixture was concentrated to 50 mL
  2. customThe reaction mixture was partitioned between H2O and EtOAc
  3. customThe aqueous layer was separated
  4. extractionextracted with EtOAc
  5. dry with materialThe combined organic extracts were dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting colorless oil (370 mg, 87%) was used without further purification

Quellen und Nachweise

ORD-Eintrag
ord-6f870a38b3e145f1b0789307f90892be
Quelldatensatz
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06211373B1

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