ChemicalBook--->CAS DataBase List--->215589-37-0

215589-37-0

215589-37-0 Structure

215589-37-0 Structure
IdentificationBack Directory
[Name]

Benzenamine, 2-ethynyl-4-methyl- (9CI)
[CAS]

215589-37-0
[Synonyms]

Benzenamine, 2-ethynyl-4-methyl-
Benzenamine, 2-ethynyl-4-methyl- (9CI)
[Molecular Formula]

C9H9N
[MDL Number]

MFCD11036439
[MOL File]

215589-37-0.mol
[Molecular Weight]

131.17
Chemical PropertiesBack Directory
[Boiling point ]

241.8±33.0 °C(Predicted)
[density ]

1.03±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[form ]

solid
[pka]

2.44±0.10(Predicted)
[InChI]

1S/C9H9N/c1-3-8-6-7(2)4-5-9(8)10/h1,4-6H,10H2,2H3
[InChIKey]

VCOACWPANOYCBP-UHFFFAOYSA-N
[SMILES]

NC1=C(C#C)C=C(C)C=C1
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Hazard InformationBack Directory
[Synthesis]

Benzenamine, 4-methyl-2-[2-(trimethylsilyl)ethynyl]-

180624-14-0

Benzenamine, 2-ethynyl-4-methyl- (9CI)

215589-37-0

General procedure for the synthesis of 2-ethynyl-4-methylaniline from the compound (CAS: 180624-14-0): to a stirred 2:1 MeOH/Et2O (250 mL) solution of 2-ethynyl-4-methylaniline (22) (11.32 g, 55.6 mmol) was added, at room temperature, K2CO3 (15.38 g, 111 mmol ). After stirring at this temperature for 1 h, the reaction mixture was diluted with water and extracted with CH2Cl2. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure to afford 2-alkynyl-4-methylaniline (23) as a light brown solid without further purification (6.79 g, 93%).1H NMR (300 MHz, CDCl3) δ 7.14 (d, J = 1.5 Hz, 1H), 6.96 (dd, J = 8.2, 1.5 Hz, 1H), 6.62 (d, J = 8.2, 1.5 Hz, 1H) 6.62 (d, J = 8.2 Hz, 1H), 4.11 (s, 2H), 3.36 (s, 1H), 2.21 (s, 3H).

[References]

[1] Patent: US2014/31559, 2014, A1. Location in patent: Paragraph 0272
[2] Journal of Organic Chemistry, 2006, vol. 71, # 9, p. 3653 - 3655
[3] Synlett, 2006, # 1, p. 65 - 68
[4] Angewandte Chemie - International Edition, 2007, vol. 46, # 12, p. 2074 - 2077
[5] Journal of Organic Chemistry, 2008, vol. 73, # 11, p. 4160 - 4165
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