2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane Basic information
- Product Name:
- 2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
- Synonyms:
-
- 2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
- 2-(3-Chlorobenzyl)
- (3-CHLOROBENZYL)BORONIC ACID PINACOL ESTER
- 1,3,2-Dioxaborolane, 2-[(3-chlorophenyl)methyl]-4,4,5,5-tetramethyl-
- CAS:
- 517920-59-1
- MF:
- C13H18BClO2
- MW:
- 252.54
- Mol File:
- 517920-59-1.mol
2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane Chemical Properties
- Boiling point:
- 298.8±23.0 °C(Predicted)
- Density
- 1.08±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- Appearance
- Colorless to light yellow Liquid
2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane Usage And Synthesis
Synthesis
104-83-6
73183-34-3
517920-59-1
Example 5: Magnesium chips (16.8 mg, 0.7 mmol) were added to the reaction system as an activator under argon protection. Catalyst Fe(acac)3 (3.5 mg, 0.010 mmol, 2 mol%), p-chlorobenzyl chloride (157 μl, 1.35 mmol) and bis(pinacolato)borate (127.0 mg, 0.5 mmol) were added sequentially to tetrahydrofuran (1 ml). The reaction was carried out at -10 °C for 5 h, followed by addition of water to terminate the reaction. The reaction mixture was extracted with ethyl acetate and the product was analyzed by gas chromatography in 81% yield.
References
[1] Chemistry Letters, 2002, # 8, p. 780 - 781
[2] Patent: CN107903281, 2018, A. Location in patent: Paragraph 0026
[3] Journal of the American Chemical Society, 2012, vol. 134, # 25, p. 10693 - 10697
[4] Journal of the American Chemical Society, 2014, vol. 136, # 27, p. 9521 - 9523
[5] Chemistry Letters, 2002, # 8, p. 780 - 781
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2-[(3-chlorophenyl)Methyl]-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane(517920-59-1)Related Product Information
- 4-Chloro-3-methoxyphenylboronic acid pinacolester
- 4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)CYCLOHEX-3-ENE-1-CARBOXYLIC ACID ETHYL ESTER
- (2-BROMOMETHYLPHENYL)BORONIC ACID, PINACOL ESTER
- 4-ISOXAZOLEBORONIC ACID PINACOL ESTER
- Ethyl 2-Methyl-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoate
- methyl 2-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
- 2-(2,5-DibroMophenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
- 3-Methoxybenzylboronic acid pinacol ester