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TERT-BUTYL-3-BROMOBENZOATE

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TERT-BUTYL-3-BROMOBENZOATE Basic information

Product Name:
TERT-BUTYL-3-BROMOBENZOATE
Synonyms:
  • 3-bromo-2-tert-butylbenzoate
  • tert-Butyl 3-bromobenzoate 95+%
  • t-Butyl-3-bromobenzoate
  • Benzoic acid, 3-broMo-, 1,1-diMethylethyl ester
  • TERT-BUTYL-3-BROMOBENZOATE
  • 3-Bromobenzoic Acid-tert-Butyl Ester
  • Tert-Butyl 3-Bromobenzoate,Canonical
CAS:
69038-74-0
MF:
C11H13BrO2
MW:
257.12
EINECS:
614-908-5
Product Categories:
  • Esters
  • Phenyls & Phenyl-Het
  • Aryl
  • Ester
  • Organohalides
  • Phenyls & Phenyl-Het
Mol File:
69038-74-0.mol
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TERT-BUTYL-3-BROMOBENZOATE Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
form 
liquid
color 
Colourless
InChI
InChI=1S/C11H13BrO2/c1-11(2,3)14-10(13)8-5-4-6-9(12)7-8/h4-7H,1-3H3
InChIKey
NPVLZVSAZXTBSR-UHFFFAOYSA-N
SMILES
C(OC(C)(C)C)(=O)C1=CC=CC(Br)=C1
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Safety Information

HS Code 
2916399090
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TERT-BUTYL-3-BROMOBENZOATE Usage And Synthesis

Synthesis

585-76-2

83766-88-5

69038-74-0

Boron trifluoride diethyl ether compound (0.31 g, 2.21 mmol) was added as m-bromobenzoic acid (0.2 g, 1.64 mmol) and 2-(tert-butoxy)pyridine (0.33 g, 2.21 mmol) after dissolution in anhydrous toluene (2 mL). The reaction mixture was stirred at room temperature for 30 min, followed by quenching the reaction with anhydrous sodium bicarbonate. The reaction mixture was diluted with ethyl acetate (30 mL) and washed sequentially with water (20 mL) and brine (20 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by fast column chromatography on silica gel with dichloromethane/hexane (0:4 to 1:4) as eluent to afford the target product tert-butyl m-bromobenzoate (5a) as a colorless oil.

References

[1] Tetrahedron, 2018, vol. 74, # 27, p. 3748 - 3754

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