(R)-(+)-1-(4-BROMOPHENYL)ETHYLAMINE Chemical Properties

Melting point:

-25°C

Boiling point:

140-145 °C (30 mmHg)

alpha 

20.5 º (C=3% IN MEOH)

Density 

1.390 g/mL at 20 °C (lit.)

refractive index 

n20/D 1.566

Flash point:

>110°C

storage temp. 

Keep in dark place,Inert atmosphere,2-8°C

pka

8.82±0.10(Predicted)

form 

clear liquid

color 

Colorless to Almost colorless

optical activity

[α]20/D +20.5±1°, c = 3% in methanol

Sensitive 

Air Sensitive

BRN 

2412319

CAS DataBase Reference

45791-36-4(CAS DataBase Reference)

NIST Chemistry Reference

(+)-P-bromo-«alpha»-phenethylamine(45791-36-4)

Safety Information

Hazard Codes 

C,N

Risk Statements 

34-51/53-22

Safety Statements 

26-28-36/37/39-45-61

RIDADR 

UN 2735 8/PG 3

WGK Germany 

3

F 

10-23

HazardClass 

8

PackingGroup 

II

HS Code 

29214990

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

(R)-(+)-1-(4-BROMOPHENYL)ETHYLAMINE Usage And Synthesis

Chemical Properties

clear colorless liquid

Synthesis

General procedure for the synthesis of 1-(4-bromophenyl)ethylamine from 1-(4-bromophenyl)ethylamine: 600 g of R-mandelic acid is added to a mixture of 2900 ml of isopropanol and 1500 ml of ethanol and heated to 60°C to dissolve completely. Subsequently 790 g of 4-bromophenethylamine is slowly added (note the exothermic reaction). After the reaction solution cooled naturally to room temperature, it was allowed to stand overnight with continuous stirring during the period. The solid product was collected by filtration and dried to give 660 g of crystals. The resulting crystals were dissolved in a mixture of 2000 ml of isopropanol and 1100 ml of ethanol, heated to 60°C to dissolve the crystals completely, and then cooled to room temperature. After standing overnight, the reaction mixture was stirred, the solid product was collected by filtration and washed with a small amount of acetone and dried to give 510 g of crystals. It was neutralized to basicity with 4M sodium hydroxide solution and subsequently extracted three times with dichloromethane. The organic phases were combined, dried and concentrated to give a final 260.7 g of colorless liquid product in 33% yield.

References

[1] Patent: CN106957255, 2017, A. Location in patent: Paragraph 0059-0061; 0073-0075; 0087-0089
[2] Chemical Communications, 2013, vol. 49, # 77, p. 8629 - 8631
[3] ChemCatChem, 2014, vol. 6, # 4, p. 992 - 995

(R)-(+)-1-(4-BROMOPHENYL)ETHYLAMINE(45791-36-4)Related Product Information

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