4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene
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
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
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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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene(461432-23-5)Related Product Information
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- Donepezil
- 1-Chloro-2-(4-ethoxybenzyl)-4-iodobenzene
- 5-Bromo-2-chlorobenzoic acid
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- (5-bromo-2-chlorophenyl)(4-ethoxyphenyl)methanone
- 4-BROMO-1-CHLORO-2-ETHYLBENZENE
- 5-bromo-2-chloro-4’-ethoxydiphenylmethane