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HYDROCORTISONI ACETAS

5-Bromo-2,3-difluorophenol

CAS: 186590-26-1

Molecular Formula: C6H3BrF2O

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HYDROCORTISONI ACETAS - Names and Identifiers

Name 5-Bromo-2,3-difluorophenol
Synonyms LANACORT
HYDROCORTONE ACETATE
Bromodifluorophenol5
HYDROCORTISONI ACETAS
5-Bromo-2,3-difluorophenol
2,3-difluoro-5-bromophenol
2,3-Difluoro-5-bromophenol
3-Bromo-5,6-difluorophenol
bis[3-(trifluoromethyl)phenyl]methanone
21-ACETOXY-4-PREGNENE-11BETA,17ALPHA-DIOL-3,20-DIONE
21-ACETOXY-4-PREGNENE-11BETA,17ALPHA,21-TRIOL-3,20-DIONE
DELTA4-PREGNEN-11BETA,17ALPHA-21-TRIOL-3,20-DIONE-ACETATE
11BETA,17ALPHA,21-TRIHYDROXY-4-PREGNENE-3,20-DIONE 21-ACETATE
CAS 186590-26-1
EINECS 606-090-3
InChI InChI=1/C6H3BrF2O/c7-3-1-4(8)6(9)5(10)2-3/h1-2,10H

HYDROCORTISONI ACETAS - Physico-chemical Properties

Molecular FormulaC6H3BrF2O
Molar Mass208.99
Density1.858±0.06 g/cm3(Predicted)
Melting Point223°C (dec.)(lit.)
Boling Point65-66°C/0.1mm
Flash Point82.1°C
Vapor Presure0.121mmHg at 25°C
BRN8831044
pKa6.75±0.15(Predicted)
Storage ConditionInert atmosphere,Room Temperature
Refractive Index1.538
Physical and Chemical PropertiesColorless transparent liquid

HYDROCORTISONI ACETAS - Risk and Safety

Risk CodesR63 - Possible risk of harm to the unborn child
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS36/37 - Wear suitable protective clothing and gloves.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
RTECSGM8960000
Hazard NoteToxic
Hazard ClassIRRITANT

HYDROCORTISONI ACETAS - Reference Information

Use 5-bromo-2, 3-difluorophenol is an important intermediate for the synthesis of a large number of compounds with physiological or pharmacological activity, the compounds can also be used in the synthesis of agrochemicals and liquid crystal compounds, and are increasingly used.
preparation (1) to a ML four-port reaction bottle equipped with a magnet and a return condenser, add 84.4g-3, 5-trifluorobromobenzene (0.4mol), 1.2 mL methanol and 67.2g
KOH (mol). After the addition, the temperature was raised to 60 ℃, and the reaction was stirred for 6H, until the raw materials are basically reacted. After the reaction, the reaction solution was frozen at -10 °c for 5h, and a large number of crystals were precipitated. The crystals were separated by Suction filtration to obtain 80.0g, the content of 3-difluoro-5-bromoanisole was 99.2%. Methanol recovery can be reused. (2) add 80.0G
2, 3-difluoro-5-bromoanisole (0.36mol) obtained above to a ML reaction flask equipped with a magnet and a reflux condenser, ML of toluene and 71.8G of AlCl3 (0.54mol). Under the protection of nitrogen, the temperature was raised to 80 ° C., the reaction was stirred for 5h, and the reaction progress was followed by gas chromatography until the basic reaction of 2, 3-difluoro-5-bromoanisole was completed. After completion of the reaction, the reaction solution was washed with water, the upper layer was separated, the toluene was removed by rotary evaporation, and distilled under reduced pressure to obtain 67.7g of 5-bromo-2, 3-difluorophenol,
The product content was 99.3% by GC analysis. The recovered toluene can be reused after drying treatment. After detection, the NMR spectrum and mass spectrum of the obtained target product were consistent with the standard sample, and the total yield of the two-step reaction was 81.0%.
Chemical properties colorless transparent liquid
Last Update:2024-04-09 21:01:54
HYDROCORTISONI ACETAS
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