Hydrochloric Acid → 5-Methoxy-2-methyl-3H-benzotellurazolium Chloride

HRID 543069Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 543069
[Cl:1][TeH:2]1(Cl)(Cl)[C:7]2[CH:8]=[CH:9][C:10]([O:12][CH3:13])=[CH:11][C:6]=2[NH+:5]=[C:4]([CH3:14])O1.[OH-].[Na+].[BH4-].[Na+].Cl>CO.O>[Cl-:1].[CH3:13][O:12][C:10]1[CH:9]=[CH:8][C:7]2[Te:2][CH:4]([CH3:14])[NH2+:5][C:6]=2[CH:11]=1

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 1317151111,1,1-Trichloro-6-methoxy-3-methyl-2,1,4-benzoxatellurazinium

Produkt 1

HCID 198452855-Methoxy-2-methyl-3H-benzotellurazolium Chloride

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

1,1,1-Trichloro-6-methoxy-3-methyl-2,1,4-benzoxatellurazinium, inner salt (Example 7) (40 g=0.1 mole) was suspended in methanol (400 ml), and a solution of sodium hydroxide (8.0 g=0.2 mole) in water (75 ml) was added. This formed a clear solution which was placed into a vessel fitted with a stirrer, a nitrogen inlet, and a condenser. Under nitrogen, sodium borohydride (10.6 g, 0.28 mole) was added in small increments until the solution no longer turned red or orange with further additions, eventually turning colorless. Partway into the reduction, the mixture solidified, but liquified again as the reduction progressed. To the suspension, which had been cooled to ≃10° C., was then added concentrated hydrochloric acid (100 ml) in one portion. The precipitate was filtered after 15 minutes (yield 42 g dark solid), and the filtrate was chilled for a second crop of 12 g solids. The first crop was recrystallized from 700 ml of hot water containing a little hydrochloric acid. The recovery was 16.1 g of almost white needles. The second crop also contained sodium chloride. It was recrystallized from 125 ml methanol, also containing a little hydrochloric acid, to give 3.6 g product. The combined yield of 19.7 g represented 63% of theory. For analysis, the material was crystallized once more from acidic methanol, 105° C. (sinter), 130°-135° C. (turned black), no clear melt >270° C.

Aufarbeitung

  1. customThis formed a clear solution which
  2. customwas placed into a vessel
  3. customfitted with a stirrer, a nitrogen inlet, and a condenser
  4. temperatureTo the suspension, which had been cooled
  5. customto ≃10° C.
  6. filtrationThe precipitate was filtered after 15 minutes (yield 42 g dark solid)
  7. temperaturethe filtrate was chilled for a second crop of 12 g solids
  8. customThe first crop was recrystallized from 700 ml of hot water containing a little hydrochloric acid
  9. customIt was recrystallized from 125 ml methanol
  10. additionalso containing a little hydrochloric acid

Quellen und Nachweise

ORD-Eintrag
ord-11f53c9dda744b12af61299ac4053dd9
Quelldatensatz
uspto-grants-1987_04
Patentnummer
US04661438

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