2,4-Difluorobenzylamine CAS NO.72235-52-0

2,4-Difluorobenzylamine CAS NO.72235-52-0

Benzene ring; organic amine compound; benzene ring series; amine; halogenated substance; organic building block; dulutvir sodium

2,4-Difluorobenzylamine Basic information

Product Name:

2,4-Difluorobenzylamine

Synonyms:

RARECHEM AL BW 0282;2,4-DIFLUOROBENZYLAMINE;2,4-DIFLUOROBENZYLAMINE HYDROCHLORIDE;2,4-Difluorobenzylamine, 98+%;(2,4-Difluorophenyl)methanamine;Benzenemethanamine, 2,4-difluoro-;2,4-Difluorobenzenemethanamine;2,4-Fluorobenzylamine

CAS:

72235-52-0

MF:

C7H7F2N

MW:

143.13

EINECS:

276-502-0

 

2,4-Difluorobenzylamine Chemical Properties

Melting point 255-256 °C(Solv: N,N-dimethylformamide (68-12-2))
Boiling point 82-84 °C (15 mmHg)
density 1.204 g/mL at 25 °C (lit.)
refractive index n20/D 1.49(lit.)
Fp 155 °F
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 8.58±0.10(Predicted)
form Liquid
color Clear colorless to light yellow
Specific Gravity 1.204
Sensitive Air Sensitive
BRN 3539259

 

2,4-Difluorobenzylamine Usage And Synthesis

Chemical Properties clear colorless to light yellow liquid
Uses 2,4-Difluorobenzylamine has been used in the synthesis of βAla–Aib(N-fluoroarylmethyl)], nonpolar nucleobase dipeptide via Ugi four-component condensation reaction.

 

A new production method

a). Using m-difluorobenzene as the starting material, it undergoes Friedel-Crafts alkylation reaction with ethylene oxide under the catalysis of Lewis acid to prepare the intermediate product 2,4‑difluorophenethyl alcohol;

b). Step a) The product is directly subjected to the second step reaction without separation and purification to oxidize 2,4‑difluorophenylethanol to generate 2,4‑difluorophenylacetic acid;

c) Step b) The product 2,4-difluorophenylacetic acid reacts with thionyl chloride and ammonia to prepare 2,4-difluorophenylacetamide;

d). Step c) The product 2,4-difluorobenzeneacetamide reacts with sodium hypochlorite aqueous solution under the induction of bromine, and Hoffman degradation occurs to prepare the target product 2,4-difluorobenzylamine

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