2-CHLORO-6-FLUORO-3-METHOXYANILINE

2-CHLORO-6-FLUORO-3-METHOXYANILINE Property

Melting point:

37-40°

Boiling point:

247.5±35.0 °C(Predicted)

Density 

1.331±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

pka

0.84±0.10(Predicted)

form 

crystalline solid

color 

White

Safety

HS Code 

2921490090

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

2-CHLORO-6-FLUORO-3-METHOXYANILINE Chemical Properties,Usage,Production

Synthesis

General procedure for the synthesis of 2-chloro-6-fluoro-3-methoxyaniline from 2-chloro-6-fluoro-3-methoxybenzoic acid: To a mixture of dichloromethane (20 mL) and N,N-dimethylformamide (3 drops), a solution of 2-chloro-6-fluoro-3-methoxylbenzoic acid (2.7 g, 13.2 mmol, 1.0 equiv.) was added drop-wise at 0 °C and oxalyl chloride ( 5.0 g, 39.6 mmol, 3.0 equiv). The reaction mixture was stirred at room temperature for 1 h and then concentrated to dryness. The residue was dissolved in acetone (20 mL) and added dropwise to a solution of sodium azide (2.6 g, 39.6 mmol, 3.0 equiv) in water (15 mL) at 0 °C. The reaction was stirred at 0 °C for 1 h. Water (50 mL) was added and the reaction mixture was then heated at 70 °C overnight. The acetone was removed by distillation and the aqueous residue was extracted with ethyl acetate. The combined organic extracts were washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated in vacuum to give the residue. The residue was purified by column chromatography (ethyl acetate: petroleum ether, 0:1 to 1:30) to give the title compound as a yellow oil (0.85 g, 37%).LC-MS: m/z 176.0, 178.0 [M + H]+.

References

[1] Patent: WO2013/37705, 2013, A2. Location in patent: Page/Page column 104; 105