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t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate

Product Name
t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate
CAS No.
123387-53-1
Chemical Name
t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate
Synonyms
1-BOC-1,2,3,4-Tetrahydroquinoline;t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate;tert-butyl 3,4-dihydro-2H-quinoline-1-carboxylate;tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate;tert-butyl 1,2,3,4-tetrahydroquinoline-1-carboxylate;1(2H)-Quinolinecarboxylic acid, 3,4-dihydro-, 1,1-dimethylethyl ester
CBNumber
CB52563650
Molecular Formula
C14H19NO2
Formula Weight
233.31
MOL File
123387-53-1.mol
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t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate Property

Boiling point:
325.9±12.0 °C(Predicted)
Density 
1.087±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
0.88±0.20(Predicted)
Appearance
Light yellow to light brown Liquid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B700730
Product name
tert-Butyl3,4-Dihydroquinoline-1(2H)-carboxylate
Packaging
100mg
Price
$75
Updated
2021/12/16
Ark Pharm
Product number
P000088205
Product name
tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate
Purity
98%
Packaging
1g
Price
$41
Updated
2021/12/16
Ark Pharm
Product number
P000088205
Product name
tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate
Purity
98%
Packaging
5g
Price
$141
Updated
2021/12/16
Ark Pharm
Product number
P000088205
Product name
tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate
Purity
98%
Packaging
10g
Price
$255
Updated
2021/12/16
AK Scientific
Product number
Z8714
Product name
1-BOC-1,2,3,4-Tetrahydroquinoline
Packaging
10g
Price
$271
Updated
2021/12/16
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t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate Chemical Properties,Usage,Production

Synthesis

635-46-1

24424-99-5

123387-53-1

GENERAL STEPS: 1,2,3,4-tetrahydroquinoline (626 mg, 4.7 mmol) was dissolved in acetonitrile (15 mL) under nitrogen protection, and triethylamine (1.3 mL, 9.3 mmol) and 4-dimethylaminopyridine (DMAP, 112 mg, 0.19 mmol) were added sequentially. Subsequently, di-tert-butyl dicarbonate (1.181 g, 5.4 mmol) was slowly added to the reaction system. The reaction mixture was stirred at room temperature for 1.5 hours and then warmed up to 55 °C to continue the reaction overnight. After completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove the solvent. The residue was extracted by partitioning with ethyl acetate (25 mL) and 1M hydrochloric acid (25 mL). The organic phase was separated and washed sequentially with 1M hydrochloric acid (2 x 25 mL) and saturated saline (25 mL). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel fast column chromatography (Combiflash system, elution gradient: 0% to 40% ethyl acetate/hexane) to afford tert-butyl 3,4-dihydroquinoline-1(2H)-carboxylate (139 mg, 13% yield) as a colorless oil.

References

[1] Chemistry - A European Journal, 2016, vol. 22, # 36, p. 12891 - 12903
[2] Patent: WO2015/48553, 2015, A1. Location in patent: Page/Page column 15; 32
[3] Tetrahedron, 2015, vol. 71, # 29, p. 4738 - 4744
[4] Organic and Biomolecular Chemistry, 2018, vol. 16, # 11, p. 1971 - 1975
[5] Chemistry - A European Journal, 2018, vol. 24, # 32, p. 8051 - 8055

t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate Preparation Products And Raw materials

Raw materials

Preparation Products

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t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate Suppliers

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123387-53-1, t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylateRelated Search:


  • 1-BOC-1,2,3,4-Tetrahydroquinoline
  • t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate
  • tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate
  • tert-butyl 1,2,3,4-tetrahydroquinoline-1-carboxylate
  • 1(2H)-Quinolinecarboxylic acid, 3,4-dihydro-, 1,1-dimethylethyl ester
  • tert-butyl 3,4-dihydro-2H-quinoline-1-carboxylate
  • 123387-53-1