3-BROMO-4-HYDROXYPHENYLACETIC ACID
3-BROMO-4-HYDROXYPHENYLACETIC ACID Basic information
- Product Name:
- 3-BROMO-4-HYDROXYPHENYLACETIC ACID
- Synonyms:
-
- 3-BROMO-4-HYDROXYBENZENEACETIC ACID
- 3-BROMO-4-HYDROXYPHENYLACETIC ACID
- 3-Bromo-4-hydroxyphenyl
- 2-(3-bromo-4-hydroxyphenyl)acetic acid
- Benzeneacetic acid, 3-bromo-4-hydroxy-
- CAS:
- 38692-80-7
- MF:
- C8H7BrO3
- MW:
- 231.04
- EINECS:
- 254-089-8
- Product Categories:
-
- Aromatic Phenylacetic Acids and Derivatives
- Organic acids
- Mol File:
- 38692-80-7.mol
3-BROMO-4-HYDROXYPHENYLACETIC ACID Chemical Properties
- Melting point:
- 105-107℃
- Boiling point:
- 364℃
- Density
- 1.757
- Flash point:
- 174℃
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 4.33±0.10(Predicted)
- CAS DataBase Reference
- 38692-80-7(CAS DataBase Reference)
3-BROMO-4-HYDROXYPHENYLACETIC ACID Usage And Synthesis
Synthesis
774-81-2
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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3-BROMO-4-HYDROXYPHENYLACETIC ACID(38692-80-7)Related Product Information
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- 3-BROMO-4-HYDROXYPHENYLACETIC ACID
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