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ChemicalBook--->CAS DataBase List--->946122-05-0

946122-05-0

946122-05-0 Structure

946122-05-0 Structure
IdentificationBack Directory
[Name]

2-AMINO-4-BROMOBENZYL ALCOHOL
[CAS]

946122-05-0
[Synonyms]

Ambroxol Impurity 52
2-AMINO-4-BROMOBENZYL ALCOHOL
2-Amino-4-bromobenzenemethanol
(2-AMINO-4-BROMOPHENYL)METHANOL
Benzenemethanol, 2-amino-4-bromo-
[Molecular Formula]

C7H8BrNO
[MDL Number]

MFCD07779492
[MOL File]

946122-05-0.mol
[Molecular Weight]

202.05
Chemical PropertiesBack Directory
[Boiling point ]

347.8±27.0 °C(Predicted)
[density ]

1.660±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

14.01±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2922190090
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-4-BROMOBENZYL ALCOHOL(946122-05-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 2-amino-4-bromobenzoate

135484-83-2

2-AMINO-4-BROMOBENZYL ALCOHOL

946122-05-0

Step 1: Methyl 2-amino-4-bromobenzoate (500 mg, 2.17 mmol) was dissolved in anhydrous THF (10 mL) and the solution was cooled to -10 °C. Under stirring, lithium aluminum hydride (1 M solution of THF, 6.5 mL, 6.52 mmol) was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was allowed to gradually warm up to room temperature and stirred at room temperature overnight. Upon completion of the reaction, the mixture was cooled in an ice-water bath and the reaction was quenched by sequential addition of methanol and saturated potassium sodium tartrate solution. The mixture was continued to be stirred at room temperature for 6 hours. Subsequently, the reaction mixture was diluted with a mixture of ethyl acetate and water to separate the organic and aqueous phases. The organic phase was dried over anhydrous magnesium sulfate, filtered, and concentrated to dryness under reduced pressure to give (2-amino-4-bromophenyl)methanol (Ex.44a, 326 mg, 74% yield) as a viscous brown solid.

[References]

[1] Patent: WO2018/138359, 2018, A1. Location in patent: Page/Page column 41; 61
[2] Journal of Organic Chemistry, 2014, vol. 79, # 3, p. 1235 - 1246
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