Sulfuric Acid → Ethanol, 2-[2-(10H-phenothiazin-10-yl)ethoxy]-

HRID 2226739Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2226739
O1CCCCC1[O:7][CH2:8][CH2:9][O:10][CH2:11][CH2:12][N:13]1[C:26]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[S:20][C:19]2[C:14]1=[CH:15][CH:16]=[CH:17][CH:18]=2.CC(O)C.S(=O)(=O)(O)O.[OH-].[Na+]>O>[CH:25]1[C:26]2[N:13]([CH2:12][CH2:11][O:10][CH2:9][CH2:8][OH:7])[C:14]3[C:19](=[CH:18][CH:17]=[CH:16][CH:15]=3)[S:20][C:21]=2[CH:22]=[CH:23][CH:24]=1

Komponenten

6

Versuchsvorschrift

A mixture of crude 10-(2-(2-((tetrahydro-2-pyranyl)oxy)ethoxy)ethyl)-10H-phenothiazine (3.8 g, 10 mmol), 2-propanol (50 ml) and a 4 M aqueous sulfuric acid solution (8 ml) was heated at 60° C. for 3 h and then left overnight at room temperature. The reaction mixture was poured into a mixture of water (500 ml) and a 4 N sodium hydroxide solution (17 ml). The mixture was extracted with diethyl ether (150 ml) and the organic extract was washed with brine and dried over sodium sulphate. The solvent was evaporated in vacuo to give 1.5 g of crude 2-(2-(10H-phenothiazin-10-yl)ethoxy)ethanol. TLC: rf=0.52 (SiO2 ; dichloromethane/methanol=19:1).

Aufarbeitung

  1. extractionThe mixture was extracted with diethyl ether (150 ml)
  2. extractionthe organic extract
  3. washwas washed with brine
  4. dry with materialdried over sodium sulphate
  5. customThe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-3887336a9a3f46b2a6c294d7d686288f
Quelldatensatz
uspto-grants-1994_09
Patentnummer
US05348965

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