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261904-39-6

261904-39-6 Structure

261904-39-6 Structure
IdentificationBack Directory
[Name]

(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid
[CAS]

261904-39-6
[Synonyms]

136665
Flutamide Impurity 11
(R)-3-bromo-2-hydroxy-2-methylpropanoic acid
(R)-3-Bromo-2-hydroxy-2-methylpropionic Acid
(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid
(2R)-3-Bromo-2-hydroxy-2-methylpropionic acid
Propanoic acid,3-bromo-2-hydroxy-2-methyl-, (2R)
(R)-3-Bromo-2-hydroxy-2-methylpropionic Acid >
(R)-3-Bromo-2-hydroxy-2-methylpropionic Acid
[Molecular Formula]

C4H7BrO3
[MDL Number]

MFCD09751022
[MOL File]

261904-39-6.mol
[Molecular Weight]

183
Chemical PropertiesBack Directory
[Melting point ]

113.0 to 117.0 °C
[Boiling point ]

294.5±25.0 °C(Predicted)
[density ]

1.831±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform, Methanol
[form ]

Solid
[pka]

3.39±0.16(Predicted)
[color ]

Off-White
[InChI]

InChI=1S/C4H7BrO3/c1-4(8,2-5)3(6)7/h8H,2H2,1H3,(H,6,7)/t4-/m0/s1
[InChIKey]

HBJAYXGUOOININ-BYPYZUCNSA-N
[SMILES]

C(O)(=O)[C@](O)(C)CBr
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/38
[Safety Statements ]

26
[RIDADR ]

UN 3261 8/PG III
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

2918199890
Hazard InformationBack Directory
[Uses]

(2R)-3-Bromo-2-hydroxy-2-methylpropionic Acid is used as a reagent in the synthesis of [18F]-radiolabeled hydroxyflutamide derivatives as prostate cancer PET imaging agents.
[Synthesis]

ALCHEMLAB AL00350

106138-80-1

(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid

261904-39-6

General procedure for the synthesis of (R)-3-bromo-2-hydroxy-2-methylpropionic acid (R-131) from the compound (CAS: 106138-80-1): bromolactone R-130 (18.5 g, 71 mmol) was dissolved in 300 mL of 24% hydrobromic acid and heated to reflux for 1 hour. After completion of the reaction, the resulting solution was diluted with 200 mL of brine and extracted with ethyl acetate (100 mL × 4). The organic phases were combined and washed with saturated sodium bicarbonate solution (100 mL × 4). The aqueous phase was acidified to pH = 1 with concentrated hydrochloric acid and extracted again with ethyl acetate (100 mL × 4). The organic phases were combined, dried with anhydrous sodium sulfate, filtered through diatomaceous earth, and concentrated to dryness under reduced pressure. The product was recrystallized from toluene to give 10.2 g (86% yield) of the target compound as colorless crystals. Melting point: 107-109 °C (S-isomer, literature value: melting point 109-113 °C).1H NMR (300 MHz, DMSO-d6) δ 3.63 (d, J=10.1 Hz, 1H, CHHa), 3.52 (d, J=10.1 Hz, 1H, CHHb), 1.35 (s, 3H, Me).IR (KBr) 3434 (OH), 3300-2500 (COOH), 1730 (C=O), 1449, 1421, 1380, 1292, 1193, 1085 cm-1. [α]D26 +10.5° (c=2.6, MeOH). Calculated elemental analysis (C4H7BrO3): C 26.25, H 3.86; measured values: C 26.28, H 3.75.

[References]

[1] Patent: US2003/225040, 2003, A1. Location in patent: Page 16
[2] Patent: US2006/9488, 2006, A1. Location in patent: Page/Page column 52
[3] Patent: WO2007/27582, 2007, A2. Location in patent: Page/Page column 61
[4] Patent: WO2007/62230, 2007, A2. Location in patent: Page/Page column 149; 151
[5] Patent: WO2008/8433, 2008, A2. Location in patent: Page/Page column 123; 1/19; 3/19; 7/19
Spectrum DetailBack Directory
[Spectrum Detail]

(2R)-3-Bromo-2-hydroxy-2-methylpropanoic acid(261904-39-6)1HNMR
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