Basic information Safety Supplier Related

(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL

Basic information Safety Supplier Related

(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL Basic information

Product Name:
(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL
Synonyms:
  • 1-(2-SULFANYLNAPHTHALEN-1-YL)NAPHTHALENE-2-THIOL
  • (+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL
  • ()-1.1''-BINAPHTHALENE-2,2''-DITHIO
  • 1,1'-Binaphthyl-2,2'-dithiol
  • 1,1'-Binaphthyl-2,2'-dithiol
  • [1,1'-binaphthalene]-2,2'-dithiol
  • (+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL
CAS:
102555-71-5
MF:
C20H14S2
MW:
318.46
Mol File:
102555-71-5.mol
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(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL Chemical Properties

Melting point:
mp 150-151 °C (benzene)
Boiling point:
495.0±40.0 °C(Predicted)
Density 
1.283±0.06 g/cm3(Predicted)
pka
5.83±0.30(Predicted)
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(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL Usage And Synthesis

Uses

1,1''-Binaphthyl-2,2''-dithiol is used in the preparation of chiral, atropisomeric organosulfur compounds.

Preparation

the original procedure of 1,1'-Binaphthyl-2,2'-dithiol used Ullman coupling of 1-bromo-2-naphthalenesulfonic acid. The intermediate 1,1′-binaphthalene-2,2′-sulfonic acid can be resolved with strychnine. Lithiation of 2,2′- dibromo-1,1′-binaphthalene with t-butyllithium, quenching with sulfur, and reduction of the resulting disulfide is an alternative preparation of the racemic dithiol. More practical procedures entail Newman-Kwart rearrangement of the thioester derived from binaphthol and dimethylthiocarbamoyl chloride, followed by hydrolysis. Use of enantiomerically pure binaphthol as starting material gives the enantiomerically pure reagent. Another resolution procedure involves enantioselective oxidation of sulfides which can be further transformed into the dithiol.

storage

(+/-)-1,1'-Binaphthyl-2,2'-dithiol oxidizes easily to the disulfide and should be stored under inert atmosphere. Use in a fume hood.

(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOLSupplier

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(+/-)-1.1'-BINAPHTHALENE-2,2'-DITHIOL(102555-71-5)Related Product Information