ChemicalBook--->CAS DataBase List--->3111-37-3

3111-37-3

3111-37-3 Structure

3111-37-3 Structure
IdentificationMore
[Name]

3-Bromo-5-ethoxy-4-hydroxybenzaldehyde
[CAS]

3111-37-3
[Synonyms]

3-BROMO-5-ETHOXY-4-HYDROXYBENZALDEHYDE
5-BROMO-3-ETHOXY-4-HYDROXYBENZALDEHYDE
AKOS B000259
ART-CHEM-BB B000259
OTAVA-BB BB7018801966
TIMTEC-BB SBB006978
3-bromo-4-hydroxy-5-ethoxybenzaldehyde
[Molecular Formula]

C9H9BrO3
[MDL Number]

MFCD00173904
[Molecular Weight]

245.07
[MOL File]

3111-37-3.mol
Chemical PropertiesBack Directory
[Melting point ]

141-143°C
[Boiling point ]

303.8±37.0 °C(Predicted)
[density ]

1.568±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

6.39±0.23(Predicted)
[Appearance]

White to off-white Solid
[Sensitive ]

Air Sensitive
[CAS DataBase Reference]

3111-37-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2913000090
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-Bromo-5-ethoxy-4-hydroxybenzaldehyde, 97%(3111-37-3)
Hazard InformationBack Directory
[Synthesis]

Phenol, 2-bromo-6-ethoxy-4-methyl-

1567388-59-3

3-Bromo-5-ethoxy-4-hydroxybenzaldehyde

3111-37-3

General procedure for the synthesis of 3-bromo-5-ethoxy-4-hydroxybenzaldehyde from the compound (CAS: 1567388-59-3): a mixture of substrate 1a (1 mmol), cobalt salt (n1 mol%), and NaOH (n2 equivalents) in ethylene glycol (EG, 5 mL) was stirred and reacted for 8 hr at 80 °C under oxygen (1 atm) atmosphere. Upon completion of the reaction, hydrochloric acid (10 mL, 2%) and methyl tert-butyl ether (MTBE, 10 mL) were sequentially added to the reaction mixture. The organic layer was separated and the aqueous phase was further extracted with MTBE (10 mL x 2). All organic phases were combined, dried with anhydrous sodium sulfate and concentrated to obtain the residue. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 10:1) to afford the target product 3-bromo-5-ethoxy-4-hydroxybenzaldehyde (2a).

[References]

[1] Tetrahedron Letters, 2014, vol. 55, # 8, p. 1406 - 1411
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