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116233-17-1

116233-17-1 Structure

116233-17-1 Structure
IdentificationBack Directory
[Name]

5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenamine
[CAS]

116233-17-1
[Synonyms]

5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenamine
3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-amine
2-Naphthalenamine, 5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-
[EINECS(EC#)]

1806241-263-5
[Molecular Formula]

C15H23N
[MOL File]

116233-17-1.mol
[Molecular Weight]

217.35
Chemical PropertiesBack Directory
[Melting point ]

96-97 °C
[Boiling point ]

321.2±31.0 °C(Predicted)
[density ]

0.938±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

5.01±0.60(Predicted)
Hazard InformationBack Directory
[Synthesis]

Naphthalene, 1,2,3,4-tetrahydro-1,1,4,4,6-pentamethyl-7-nitro-

116233-16-0

5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenamine

116233-17-1

3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-amine (6) was synthesized as follows: 1,1,4,4,6-pentamethyl-7-nitro-1,2,3,4-tetrahydronaphthalene (5) (2.5 g, 10.1 mmol) was dissolved in ethyl acetate (205 mL) to prepare a 0.05 M solution. The hydrogenation reaction was repeated twice using a ThalesNano H-cube?reactor at 70°C and 2-5 bar pressure through a 10 mL Pd/C cartridge at a flow rate of 1.0 mL/min. Upon completion of the reaction, the resulting solution was concentrated under vacuum to afford the target product 6 (2.13 g, 97% yield) as a yellow crystalline solid with a melting point of 205°C. The structure of the product was confirmed by the following characterization data: 1H NMR (400 MHz, CDCl3) δ 7.00 (s, 1H), 6.63 (s, 1H), 3.34 (br s, 2H), 2.15 (s, 3H), 1.63 (s, 4H), 1.26 (s, 12H); 13C NMR (100.6 MHz, CDCl3) δ 143.5, 142.0, 135.2, 128.3, 120.5, 112.6, 35.3, 35.2, 33.8, 33.4, 32.0, 31.8, 17.1; IR ( neat)ν 3404, 3335, 2956, 2925, 1626, 1504 cm-1; LC-MS-CI (M+H)+ calculated value C15H24N 218.1909, measured value 218.1908.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 9, p. 2352 - 2356
[2] Patent: WO2015/130973, 2015, A1. Location in patent: Page/Page column 20; 21
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 19, p. 8924 - 8940
[4] Patent: US2018/207156, 2018, A1. Location in patent: Paragraph 0114; 0131
[5] Journal of Medicinal Chemistry, 1989, vol. 32, # 7, p. 1504 - 1517
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