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Water → 4-Isocyanatobenzene-1-thiol

HRID 616699
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 616699
C([S:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-])=O)=[CH:8][CH:7]=1)(C)(C)C.O.C(SC1C=CC(N)=CC=1)(C)(C)C.[C:28](Cl)(Cl)=[O:29]>[Fe].C1C=CC=CC=1.C(O)(=O)C>[SH:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]=[C:28]=[O:29])=[CH:8][CH:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 962WaterHCID 6371PhosgeneHCID 109101774-(Tert-butylsulfanyl)anilineHCID 129583221-((1,1-Dimethylethyl)thio)-4-nitrobenzene

Produkt 1

HCID 190755954-Isocyanatobenzene-1-thiol

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23925Iron
Katalysator
HCID 176Acetic AcidLösungsmittel
HCID 241BenzeneLösungsmittel2×

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a suspension of 4-(t-butylmercapto)nitrobenzene (52.8 g., 0.25 mol) and iron powder (150 g.) in 1 l. of water there was added 1 ml. of acetic acid. The reaction mixture was stirred 18 hours at 90° C. and filtered. Both the residue and filtrate were extracted several times with methylene dichloride, and the combined dried methylene dichloride extracts were concentrated at reduced pressure to give 18.2 g. of a brown oil. This is a 40% weight yield of 4-(t-butylmercapto)aniline. To this oil in 100 ml. of benzene there was then added dropwise 158 g. of a 12.5% benzene solution of phosgene (0.2 mol) with cooling. The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature and then at reflux temperature for 7 hours. After standing overnight the reaction mixture was filtered, the filtrate concentrated at reduced pressure, then vacuum-distilled. Two product fractions were collected as

Aufarbeitung

  1. filtrationfiltered
  2. extractionBoth the residue and filtrate were extracted several times with methylene dichloride
  3. concentrationwere concentrated at reduced pressure
  4. customto give 18.2 g
  5. stirringThe reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature
  6. temperatureat reflux temperature for 7 hours
  7. waitAfter standing overnight
  8. filtrationthe reaction mixture was filtered
  9. concentrationthe filtrate concentrated at reduced pressure
  10. distillationvacuum-distilled
  11. customTwo product fractions were collected as

Quellen und Nachweise

ORD-Eintrag
ord-cf72c76e56fb436d9add06f9f7dfe9d2
Quelldatensatz
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04075345

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