ChemicalBook--->CAS DataBase List--->912347-94-5

912347-94-5

912347-94-5 Structure

912347-94-5 Structure
IdentificationBack Directory
[Name]

2-Methyl-3-amino-4-acetylanisole
[CAS]

912347-94-5
[Synonyms]

2-methyl-3-amino-4-acetylanisole
6-ACETYL-3-METHOXY-2-METHYL ANILINE
1-(2-aMino-4-Methoxy-3-Methylphenyl)-
2-AMino-4-Methoxy-3-Methylacetophenone
2-Amino-4-methoxy-3-methylbenzoic acid
(2-Amino-3-methyl-4-methoxyphenyl)acetone
2'-Amino-3'-methyl-4'-methoxyacetophenone
2-Methyl-3-amino-4-acetylanisole USP/EP/BP
1-(2-Amino-4-methoxy-3-methylphenyl)ethanone
Ethanone, 1-(2-amino-4-methoxy-3-methylphenyl)-
1-(2-aMino-4-Methoxy-3-Methylphenyl)ethan-1-one
1-(2-Amino-4-methoxy-3-methylphenyl)ethanone 97%
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C10H13NO2
[MDL Number]

MFCD11042290
[MOL File]

912347-94-5.mol
[Molecular Weight]

179.22
Chemical PropertiesBack Directory
[Melting point ]

107 °C
[Boiling point ]

336.0±37.0 °C(Predicted)
[density ]

1.096±0.06 g/cm3(Predicted)
[storage temp. ]

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

powder to crystal
[pka]

1.74±0.10(Predicted)
[color ]

White to Yellow to Orange
[InChI]

InChI=1S/C10H13NO2/c1-6-9(13-3)5-4-8(7(2)12)10(6)11/h4-5H,11H2,1-3H3
[InChIKey]

VXBGCEDOGYNWHE-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=CC=C(OC)C(C)=C1N)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2922500090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methyl-3-amino-4-acetylanisole(912347-94-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Acetonitrile

75-05-8

3-Methoxy-2-methylaniline

19500-02-8

2-Methyl-3-amino-4-acetylanisole

912347-94-5

To a solution of 2-methyl-3-methoxyaniline (5.0 g, 36.5 mmol) in p-xylene (80 mL) was cooled to 0 °C, and a dichloromethane solution (36.5 mL) of 1 M BCl3 was slowly added. The reaction mixture was stirred at 0 °C for 30 min under nitrogen protection. Subsequently, acetonitrile (2.6 mL, 54.7 mmol) was added and stirring was continued at 0 °C for 30 min. In another reaction flask, AlCl3 (4.87 g, 36.5 mmol) was suspended in anhydrous dichloromethane (50 mL), cooled to 0 °C, and the aforementioned p-xylene solution was added dropwise through the addition funnel under nitrogen protection. After addition, the dichloromethane was removed under vacuum after stirring at 0°C for 45 minutes. The remaining p-xylene solution was heated to 70°C and maintained for 18 hours, followed by cooling to room temperature. Water (80 mL) was added and again heated to 70°C maintained for 1 hour and cooled to room temperature. The reaction mixture was diluted with ethyl acetate and the aqueous layer was separated. The organic layer was washed sequentially with equal volumes of water and saturated saline, dried over anhydrous MgSO4 and concentrated under reduced pressure. 1H), 7.03 (br.s., 2H), 7.65 (d, J = 9.04 Hz, 1H). LC-MS (ESI): m/z 180.10 (M + H)+.

[References]

[1] Patent: US2010/196321, 2010, A1. Location in patent: Page/Page column 20
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 7, p. 3021 - 3026
[3] Patent: WO2008/96002, 2008, A1. Location in patent: Page/Page column 82-83
[4] Patent: WO2008/92954, 2008, A2. Location in patent: Page/Page column 28-29
[5] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 17, p. 4853 - 4858
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