ChemicalBook--->CAS DataBase List--->878671-94-4

878671-94-4

878671-94-4 Structure

878671-94-4 Structure
IdentificationBack Directory
[Name]

1-Naphthalenamine, 4-cyclopropyl-
[CAS]

878671-94-4
[Synonyms]

1-phthalemine, 4-cyclopropyl-
4-cyclopropyl-1-naphthalamine
4- cyclopropyl-1-naphthylamine
4-Cyclopropyl-1-Naphthalenamine
4-Cyclopropylnaphthalen-1-aMine
1-amino-4-cyclopropylnaphthalene
1-Naphthalenamine, 4-cyclopropyl-
4- cyclopropyl-1-naphthylamine oxalate
4-Cyclopropyl-1-naphthalenaMine oxalate
[EINECS(EC#)]

200-001-8
[Molecular Formula]

C13H13N
[MDL Number]

MFCD11109543
[MOL File]

878671-94-4.mol
[Molecular Weight]

183.25
Chemical PropertiesBack Directory
[Boiling point ]

361.6±21.0 °C(Predicted)
[density ]

1.191
[storage temp. ]

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

4.62±0.10(Predicted)
Questions And AnswerBack Directory
[Uses]

4-Cyclopropyl-1-naphthylamine is an amine derivative that can be used as an intermediate in organic synthesis.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

4-Bromo-1-naphthylamine

2298-07-9

Cyclopropylboronic acid

411235-57-9

1-Naphthalenamine, 4-cyclopropyl-

878671-94-4

Tetrakis(triphenylphosphine)palladium (0.26 g, 0.23 mmol) and potassium phosphate (1.67 g, 7.87 mmol) were added to a 50 mL round-bottomed flask under nitrogen protection using 4-bromo-1-naphthylamine (0.50 g, 2.25 mmol) and cyclopropylboronic acid (0.212 g, 2.47 mmol). A solvent mixture of dioxane and water (25:1, 26 mL) was then added, and after three nitrogen displacements, the reaction mixture was heated to reflux in a 90 °C oil bath for 6 hours. After completion of the reaction, it was cooled to room temperature and filtered to remove insoluble material. The filtrate was concentrated under reduced pressure to remove the solvent, diluted with 50 mL of water and extracted with ethyl acetate (2 x 10 mL). The organic layers were combined, washed twice with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to give the intermediate 4-cyclopropyl-1-aminonaphthalene as a purplish red oil in 95.3% yield.

[References]

[1] Chemical Biology and Drug Design, 2016, vol. 88, # 2, p. 241 - 253
[2] Patent: CN105175414, 2017, B. Location in patent: Paragraph 0040
[3] Patent: CN105566237, 2016, A. Location in patent: Paragraph 0060; 0061; 0062
[4] Patent: CN106083847, 2016, A. Location in patent: Paragraph 0133; 0134; 0170; 0171
[5] Patent: WO2006/26356, 2006, A2. Location in patent: Page/Page column 35-36
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