ChemicalBook--->CAS DataBase List--->38692-80-7

38692-80-7

38692-80-7 Structure

38692-80-7 Structure
IdentificationMore
[Name]

3-BROMO-4-HYDROXYPHENYLACETIC ACID
[CAS]

38692-80-7
[Synonyms]

3-BROMO-4-HYDROXYBENZENEACETIC ACID
3-BROMO-4-HYDROXYPHENYLACETIC ACID
3-Bromo-4-hydroxyphenyl
[EINECS(EC#)]

254-089-8
[Molecular Formula]

C8H7BrO3
[MDL Number]

MFCD00016833
[Molecular Weight]

231.04
[MOL File]

38692-80-7.mol
Chemical PropertiesBack Directory
[Melting point ]

105-107℃
[Boiling point ]

364℃
[density ]

1.757
[Fp ]

174℃
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.33±0.10(Predicted)
[CAS DataBase Reference]

38692-80-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

22
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Synthesis]

3-BROMO-4-METHOXYPHENYLACETIC ACID

774-81-2

3-BROMO-4-HYDROXYPHENYLACETIC ACID

38692-80-7

Step (b) 3-bromo-4-methoxyphenylacetic acid (14.0 g, 0.057 mol) and anhydrous dichloromethane (100 mL) were added to a 250 mL round bottom flask. The reaction mixture was degassed by nitrogen bubbling for 5 min. Subsequently, a dichloromethane solution of 1 M boron tribromide (63 mL, 0.063 mol) was added slowly and dropwise through the addition funnel. The reaction mixture was stirred at room temperature and a white solid was observed to precipitate gradually. After the reaction was carried out for 2 h, the product was separated by filtration and the collected white crystals were washed several times with dichloromethane to finally obtain 3-bromo-4-hydroxyphenylacetic acid (12 g, 92% yield).

[References]

[1] Patent: US2003/114457, 2003, A1
[2] Patent: WO2004/62661, 2004, A1. Location in patent: Page/Page column 28
[3] Patent: US2009/197959, 2009, A1. Location in patent: Page/Page column 14; 15
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