ChemicalBook--->CAS DataBase List--->30433-92-2

30433-92-2

30433-92-2 Structure

30433-92-2 Structure
IdentificationBack Directory
[Name]

CHEMBRDG-BB 4004130
[CAS]

30433-92-2
[Synonyms]

AKOS ISYA01283
CHEMBRDG-BB 4004130
RARECHEM AN KA 0153
UKRORGSYN-BB BBV-182415
2-Thiopheneethanamine, 5-methyl-
2-(5-METHYL-2-THIENYL)ETHANAMINE
2-(5-methylthiophen-2-yl)ethanamine
2-(5-METHYL-THIOPHEN-2-YL)-ETHYLAMINE
2-(5-methyl-2-thienyl)ethanamine(SALTDATA: FREE)
[Molecular Formula]

C7H11NS
[MDL Number]

MFCD08059759
[MOL File]

30433-92-2.mol
[Molecular Weight]

141.23
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C(protect from light)
Safety DataBack Directory
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Synthesis]

Thiophene, 2-methyl-5-[(1E)-2-nitroethenyl]-

117693-20-6

CHEMBRDG-BB 4004130

30433-92-2

b) Step 2: Synthesis of 2-(5-methyl-2-thienyl)ethylamine A solution of 6.9 g (175 mmol) of 2-methyl-5-((E)-2-nitrovinyl)-thiophene dissolved in 150 mL of diethyl ether was slowly added dropwise to a suspension of 6.9 g (40.78 mmol) of LiAlH4 in 70 mL of ethyl ether under nitrogen protection, controlling the temperature to 20 to 25 °C. After dropwise addition, the reaction mixture was heated to reflux for 5 hours. After completion of the reaction, the mixture was cooled to 0 °C and the reaction was quenched by sequentially adding 28 mL of water and 7 mL of 5N NaOH solution. The white solid was removed by filtration and the filter cake was washed with ethyl acetate. The filtrates were combined and concentrated under reduced pressure to remove the solvent. The residue was purified by distillation under reduced pressure to give 4.98 g (86% yield) of the target compound 2-(5-methyl-2-thienyl)ethylamine as a colorless liquid.MS (m/e): 142.2 (MH+).

[References]

[1] Patent: US2008/249125, 2008, A1. Location in patent: Page/Page column 11-12
[2] Journal of Organic Chemistry, 1950, vol. 15, p. 807,810
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