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Nitric Acid → HCID 14746146, Verbindung

HRID 1087998
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1087998
[OH:1][CH2:2][CH2:3][S:4]([CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][S:15]([CH2:18][CH2:19][OH:20])(=[O:17])=[O:16])=[CH:10][CH:9]=1)(=[O:6])=[O:5].S(=O)(=O)(O)O.[N+:26]([O-])([OH:28])=[O:27]>O>[OH:1][CH2:2][CH2:3][S:4]([CH2:7][C:8]1[CH:9]=[CH:10][C:11]([CH2:14][S:15]([CH2:18][CH2:19][OH:20])(=[O:17])=[O:16])=[CH:12][C:13]=1[N+:26]([O-:28])=[O:27])(=[O:6])=[O:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 944Nitric AcidHCID 1118Sulfuric Acid2×HCID 14746145HCID 14746145, Verbindung

Produkt 1

HCID 14746146HCID 14746146, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

80.5 parts of 1,4-bis(hydroxyethylsulfonylmethyl)benzene are stirred into 612.5 parts of 100% strength sulfuric acid, and the mixture is heated at 35° to 40° C. until a sample shows quantitative esterification in the HPLC chromatogram (about 4 to 5 hours). 57 parts of a mixture of 30 parts by weight of 100% strength nitric acid and 70 parts by weight of 100% strength sulfuric acid (so-called "M3 acid") are then added dropwise over a period of 4 hours at 30° to 40° C., stirring is continued for 2 hours at 45° C. until the nitration is completed (checked by HPLC chromatogram), and the reaction mixture is then decomposed by pouring it into 2,500 parts of cold water. The resulting aqueous acidic solution is then refluxed (about 110° C.) for 5 hours to hydrolyze the sulfuric ester groups, 5 parts of activated carbon are then added, the mixture is clarified and the clarified filtrate is cooled to 0° to 5° C. with stirring. The resulting precipitate is filtered off with suction, washed neutral and dried in vacuo at 80° C. This gives 89.0 parts of 2,5-bis(hydroxyethylsulfonylmethyl)nitrobenzene of the formula ##STR20## in the form of colorless crystals of melting point 125° to 126.5° C., the purity of which (HPLC) is 98.8%.

Aufarbeitung

  1. temperaturethe mixture is heated at 35° to 40° C. until a sample
  2. customin the HPLC chromatogram (about 4 to 5 hours)
  3. additionare then added dropwise over a period of 4 hours at 30° to 40° C.
  4. additionare then added
  5. temperaturethe clarified filtrate is cooled to 0° to 5° C.
  6. stirringwith stirring
  7. filtrationThe resulting precipitate is filtered off with suction
  8. washwashed neutral
  9. customdried in vacuo at 80° C

Quellen und Nachweise

ORD-Eintrag
ord-abbca7223da8407ca3aeb84fba867156
Quelldatensatz
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04960940

Notizen zur Reaktion

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