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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene

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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Basic information

Product Name:
4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene
Synonyms:
  • 5-bromo-2-chloro-4’-ethoxydiphenylmethane
  • Benzene, 4-bromo-1-chloro-2-[(4-ethoxyphenyl)methyl]-
  • 4-(5-Bromo-2-chlorobenzyl)phenyl ethyl ether
  • Dapagliflozin Intermediate 1
  • 4-broMo-1-chloro-2-[(4-ethoxyphenyl)Methyl]-
  • 2-(4-Methoxybenzyl)-4-broMo-1-chlorobenzene
  • 1-(5-broMo-2-chlorobenzyl)-4-ethoxybenzene
  • Dapagliflozin-13
CAS:
461432-23-5
MF:
C15H14BrClO
MW:
325.63
EINECS:
636-921-5
Product Categories:
  • Halides
  • Phenyls & Phenyl-Het
  • 461432-23-5
  • ADVANCED INT.
Mol File:
461432-23-5.mol
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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Chemical Properties

Boiling point:
393.0±32.0 °C(Predicted)
Density 
1.371±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Low-Melting Solid
color 
White to Off-White
Stability:
Stable under recommended storage conditions., Stable Under Recommended Storage C
InChI
InChI=1S/C15H14BrClO/c1-2-18-14-6-3-11(4-7-14)9-12-10-13(16)5-8-15(12)17/h3-8,10H,2,9H2,1H3
InChIKey
ZUNCHZBITMUSRD-UHFFFAOYSA-N
SMILES
C1(Cl)=CC=C(Br)C=C1CC1=CC=C(OCC)C=C1
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Safety Information

HS Code 
2909309090
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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Usage And Synthesis

Uses

5-Bromo-2-chloro-4'-ethoxydiphenylmethane is a hydrocarbon derivative and can be used as an intermediate for dapagliflozin.

Synthesis

Oxalyl chloride (0.8 mL) was added to a solution of 5-bromo-2-chlorobenzoic acid (2 g) in dichloromethane (20 mL) and dimethylformamide (0.2 mL) under a nitrogen atmosphere. The reaction mixture was stirred for one hour at 25° C to 30° C. After completion of the reaction, the reaction mixture was concentrated under a vacuum at 40° C to 45° C. to obtain an oily residue. The oily residue was dissolved in dichloromethane (20 mL) and cooled to 0° C. To this solution, phenol (1.1 mL) and aluminium chloride (2.3 g) were added at 0° C. to 5° C. The reaction mixture was stirred at 0° C to 5° C for 2 hours. The reaction mixture was allowed to warm to about 20° C, and triethylsilane (3.4 mL) was slowly added to it at the same temperature. The reaction mixture was stirred for about 36 hours from 20° C to 25° C. After completion of the reaction, 4-bromo-1-chloro-2-(4-ethoxybenzyl)benzene was obtained by further purification.

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