Reaktion #580204

Reaktionsgleichung

borate

HCl

water

6-bromo-1,2,3,4-tetrahydronaphthalene

→

1,2,3,4-tetrahydronaphthalene-6-boronic acid

Ausbeute 54.0%

Lösungsmittel

THF

hexane

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGby stirring for 2 hours at −67° C. or below
2. 2
   TemperaturThe reaction mixture was gradually warmed to room temperature
3. 3
   workup.WAITleft
4. 4
   workup.WAITstanding overnight
5. 5
   SonstigeThe resultant reaction mixture
6. 6
   Sonstigekept at 10° C. or below
7. 7
   workup.STIRRINGby stirring for 1 hour at that temperature
8. 8
   ExtraktionThereafter, the mixture was subjected to extraction with toluene
9. 9
   WaschenThe organic layer was washed with water
10. 10
    Sonstigeto obtain a residue
11. 11
    SonstigeThe residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=2/1)
12. 12
    Sonstigerecrystallized from hexane

Vorschrift

In a 5 liter three-necked flask, 67.55 g of 6-bromo-1,2,3,4-tetrahydronaphthalene and 1480 ml of dry tetrahydrofurah (THF) were placed and cooled to −70 to −68° C. on a dry ice-acetone bath in a dry nitrogen gas atmosphere. At that temperature, to the mixture, 200 ml of 1.6 M-butyllithium solution in hexane was added dropwise, followed by stirring for 2 hours at −67° C. or below. To borate in 435 ml of dry THF was added dropwise at −70 to −68° C., followed by stirring for 2 hours at −67° C. or below. The reaction mixture was gradually warmed to room temperature and left standing overnight. The resultant reaction mixture was gradually added dropwise to a mixture of 108 ml of HCl and 438 ml of water kept at 10° C. or below, followed by stirring for 1 hour at that temperature. Thereafter, the mixture was subjected to extraction with toluene. The organic layer was washed with water, followed by distilling-off of the solvent under reduced pressure to obtain a residue. The residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=2/1) and recrystallized from hexane to obtain 30.4 g of 1,2,3,4-tetrahydronaphthalene-6-boronic acid (Yield: 54.0%).

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