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1-ETHOXY-2,3-DIFLUOROBENZENE

2,3-DIFLUOROETHOXYBENZENE

CAS: 121219-07-6

Molecular Formula: C8H8F2O

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1-ETHOXY-2,3-DIFLUOROBENZENE - Names and Identifiers

Name 2,3-DIFLUOROETHOXYBENZENE
Synonyms 2,3-DIFLUOROETHOXYBE
2,3-Difluorophenetole
2,3-DIFLUOROETHOXYBENZENE
1-Ethoxy-2,3-difluorbenzol
2,3-difluoro-1-ethoxybenzene
1-ETHOXY-2,3-DIFLUOROBENZENE
2,3-DIFLUORO-4-ETHOXYBENZENE
2,3-Difluorophenyl ethyl ether
BENZENE, 1-ETHOXY-2,3-DIFLUORO-
2,3-Difluoroethoxybenzene 1-Ethoxy-2,3-difluorobenzene
CAS 121219-07-6
EINECS 441-000-4
InChI InChI=1/C8H8F2O/c1-2-11-7-5-3-4-6(9)8(7)10/h3-5H,2H2,1H3
InChIKey AVOGLGBKOFOSBN-UHFFFAOYSA-N

1-ETHOXY-2,3-DIFLUOROBENZENE - Physico-chemical Properties

Molecular FormulaC8H8F2O
Molar Mass158.15
Density1.1784
Boling Point178
Flash Point70.5
Water Solubility254mg/L at 20℃
Vapor Presure4.13hPa at 20℃
Appearanceclear liquid
ColorColorless to Light yellow
Storage ConditionSealed in dry,Room Temperature
Refractive Index1.4670-1.4710
Physical and Chemical PropertiesStorage Conditions: Keep Cold

1-ETHOXY-2,3-DIFLUOROBENZENE - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37 - Wear suitable gloves.
HS Code29093090

1-ETHOXY-2,3-DIFLUOROBENZENE - Reference Information

LogP2.82 at 23℃
Introduction 2, 3-difluorophenyl ether is liquid at normal temperature and pressure, with aromatic odor, it is insoluble in water, soluble in alcohol and ether, stable to alkali and dilute acid. 2, 3-difluorophenyl ether belongs to the basic organic raw materials of ethers, is a synthetic intermediate of pharmaceutical molecules and liquid crystal materials, and can also be used as a cosolvent for organic reactions.
Applications 2, 3-difluorophenethyl ether has been widely used in the synthesis of liquid crystal materials, in addition, in the synthetic transformation, the 4th position on the benzene ring can introduce a halogen atom including bromine, iodine and chlorine under appropriate conditions. In addition, the ethoxy group can be removed from the ethyl group by the action of the boron trifluoride ethyl ether solution to obtain a simple phenolic hydroxyl group.
synthetic method
2, 3-difluorophenol
(103.3g, 793.9 mmol) A solution of 2-butanone (770 ml) was added to potassium carbonate (128g, 923 mmol)
, and with stirring, ethyl iodide (180g,1154mmol) was added. A solution in 2-butanone (350ml), and the suspension mixture was stirred under reflux for 3 hours, and water (200ml) and toluene (100 ml) were added to the reaction mixture at room temperature,
2N sodium hydroxide (100 ml) and brine (100 ml)
The separated organic phase liquids were washed separately, and the combined organic layers were dried over anhydrous magnesium sulfate, the organic solvent was evaporated under reduced pressure and the residue was finally purified by distillation under reduced pressure to give 2, 3-difluorophenyl ether.
route for the synthesis of 2, 3-difluorophenyl ether
Last Update:2024-04-09 02:00:04
1-ETHOXY-2,3-DIFLUOROBENZENE
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View History
1-ETHOXY-2,3-DIFLUOROBENZENE
Propanoic acid, 2,3-difluoro-, methyl ester
(1S,2S)-Trans-2-Aminocyclopentanol Hydrochloride
ETHYL 4-HYDROXY-6-METHOXY-3-QUINOLINECARBOXYLATE
(E)-4-Decenal
3-(Adamantan-2-ylidene)thietan-2-one
(S)-(-)-5,5-DIMETHYL-4-PHENYL-2-OXAZOLIDINONE
THIODIGLYCOL SULFOXIDE
Ethyl D-pyroglutamate
Alprostadil (Prostaglandin E1) EP Impurity I
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