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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  Carboxylic acid esters and derivatives >  6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine

6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine

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6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine Basic information

Product Name:
6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine
Synonyms:
  • 6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine
  • tert-butyl 4,5-dihydrothieno[2,3-c]pyridine-6(7H)-carboxylate
  • tert-Butyl 4,5-dihydrothieno[2,3-c]pyridine-6(7H)
  • tert-butyl 4h,5h,6h,7h-thieno[2,3-c]pyridine-6-carboxylate
  • Thieno[2,3-c]pyridine-6(5H)-carboxylic acid, 4,7-dihydro-, 1,1-dimethylethyl ester
  • 6-Boc-4,5,6,7-tetrahydrothieno[2,3-c]pyridine
CAS:
165947-52-4
MF:
C12H17NO2S
MW:
239.33
Mol File:
165947-52-4.mol
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6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine Chemical Properties

Boiling point:
339.1±42.0 °C(Predicted)
Density 
1.173±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-1.55±0.20(Predicted)
Appearance
White to off-white Solid
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6-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-6H-thieno[2,3-c]pyridine Usage And Synthesis

Synthesis

24424-99-5

28783-38-2

165947-52-4

4,5,6,7-tetrahydrothieno[2,3-c]pyridine hydrochloride (15.0 g, 85.38 mmol) and triethylamine (24.0 mL, 170.77 mmol) were used as raw materials and dissolved in dichloromethane (150 mL). Subsequently, di-tert-butyl dicarbonate (22.36 g, 102.46 mmol) was added to the reaction system. The reaction mixture was stirred at room temperature for 4.5 hours. Upon completion of the reaction, the reaction system was quenched by adding water (50 mL) to the reaction system and subsequently extracted with dichloromethane (30 mL x 2). The organic phases were combined and washed sequentially with water (20 mL × 2) and saturated brine (30 mL), and the organic layer was dried with anhydrous sodium sulfate. After filtration, the solvent was removed by evaporation under reduced pressure, and the crude product obtained was purified by column chromatography (petroleum ether/ethyl acetate, v/v = 20/1) to finally obtain the white solid product tert-butyl 4,5-dihydrothieno[2,3-c]pyridine-6(7H)-carboxylate (20.49 g, 100% yield).

References

[1] Patent: CN104497008, 2016, B. Location in patent: Paragraph 0242; 0244; 0245

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