Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Amides >  Naphthenic amines derivatives >  1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE

1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE

Basic information Uses Safety Supplier Related

1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE Basic information

Product Name:
1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE
Synonyms:
  • 1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE
  • 1-(4-BROMOPHENYL)CYCLOPROPANAMINE
  • Cyclopropanamine, 1-(4-bromophenyl)-
  • 1-(4-bromophenyl)cyclopropan-1-amine
  • 1-(4-BROMOPHENYL)CYCLOPROPANAMINE HCL
  • 1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE ISO 9001:2015 REACH
CAS:
345965-54-0
MF:
C9H10BrN
MW:
212.09
Mol File:
345965-54-0.mol
More
Less

1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE Chemical Properties

storage temp. 
2-8°C(protect from light)
Appearance
White to light yellow Solid-liquid mixture
More
Less

1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINE Usage And Synthesis

Uses

1-(4-bromobenzene)cyclopropylamine is an amine compound that can be used as a pharmaceutical synthesis intermediate.

Synthesis

623-00-7

925-90-6

345965-54-0

General Method G: Cyclopropanation Reaction (0459) Ethylmagnesium bromide (3.0 M ethyl ether solution, 1.1 eq.) was added slowly and dropwise to a stirred mixture of arylonitrile (1 eq.) and tetraisopropoxytitanium (1.7 eq.) at -70 °C. The reaction mixture was gradually warmed to 25 °C and stirred continuously for 1 hour. Subsequently, boron trifluoride ethyl ether complex (3 eq.) was added dropwise to the reaction system at 25 °C. After the dropwise addition was completed, stirring of the reaction mixture was continued for 2 hours. After completion of the reaction, the reaction was quenched with 2M aqueous hydrochloric acid. Next, the pH of the reaction solution was adjusted to alkaline with 2M aqueous sodium hydroxide solution. The organic material in the reaction solution was extracted with ether. The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, ratio from 10:1 to 1:1 gradient elution) to obtain the target product 1-arylcyclopropylamine. Example 64: Synthesis of quinuclidinyl cyclic-3-yl 1-(biphenyl-4-yl)cyclopropyl carbamate 4-Bromobenzonitrile (3.00 g, 16.5 mmol) was converted to 1-(4-bromophenyl)cyclopropylamine (1.80 g, 51% yield) according to General Method G. The product was a yellow solid.

References

[1] Patent: US9126993, 2015, B2. Location in patent: Page/Page column 49; 87
[2] Patent: WO2016/145046, 2016, A1. Location in patent: Page/Page column 64; 65; 70; 71

1-(4-BROMO-PHENYL)-CYCLOPROPYLAMINESupplier

Jinan Demai Medical Technology Co., LTD Gold
Tel
15209235325 18669728830
Email
865681093@qq.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Email
isenchem@163.com
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Email
3007715519@qq.com