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3-tert-Butoxycarbonylphenylboronic acid

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3-tert-Butoxycarbonylphenylboronic acid Basic information

Product Name:
3-tert-Butoxycarbonylphenylboronic acid
Synonyms:
  • T-BUTYL 3-BORONOBENZOATE
  • 3-(T-BUTOXYCARBONYL)PHENYLBORONIC ACID
  • 3-(TERT-BUTOXYCARBONYL)BENZENEBORONIC ACID
  • 3-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID
  • [3-[(2-methylpropan-2-yl)oxy-oxomethyl]phenyl]boronic acid
  • 3-(Tert-Butoxycarbonyl)Phenylb
  • 3-(tert-Butoxycarbonyl)benzeneboronic acid 98%
  • 3-(T-BUTOXYCARBONYL)PHENYLBORBONIC ACID
CAS:
220210-56-0
MF:
C11H15BO4
MW:
222.05
EINECS:
691-957-9
Product Categories:
  • blocks
  • BoronicAcids
  • Carboxes
  • Boronic acids
Mol File:
220210-56-0.mol
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3-tert-Butoxycarbonylphenylboronic acid Chemical Properties

Melting point:
96-102°C
Boiling point:
375.0±44.0 °C(Predicted)
Density 
1.15±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
7.72±0.10(Predicted)
color 
White to Almost white
CAS DataBase Reference
220210-56-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-60-37
Hazard Note 
Irritant/Keep Cold
HS Code 
29319000
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3-tert-Butoxycarbonylphenylboronic acid Usage And Synthesis

Chemical Properties

White to light yellow crystal powde

Preparation

The 10L glass reactor is equipped with mechanical stirring, thermometer and constant pressure dropping funnel. Under nitrogen protection, add 3 moles of raw material m-carboxybenzene boric acid and 4kg tetrahydrofuran. Add 4.5 moles of thionyl chloride dropwise under reflux and stirring, react for 4 hours, cool to 0-5°C, add 7.5 moles of potassium tert-butoxide in batches, continue stirring for 1 hour after the addition, add 2kg of water, and acidify with acetic acid. Let sit and let the liquid separate. The organic phase was concentrated to obtain a crude product, which was recrystallized by adding 2 kg of petroleum ether to obtain a solid product, 3-tert-Butoxycarbonylphenylboronic acid, with a purity of 98% and a molar yield of 95%.

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