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4-BROMO-5-METHYL-THIOPHENE-2-BORONIC ACID PINACOL ESTER synthesis

2synthesis methods
29421-73-6 Synthesis
3,5-DIBROMO-2-METHYLTHIOPHENE

29421-73-6
92 suppliers
$19.00/1g

61676-62-8 Synthesis
2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

61676-62-8
310 suppliers
$10.00/5g

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Yield: 84%

Reaction Conditions:

with n-butyllithium in diethyl ether

Steps:

synthesis of compound (7)
Next, the compound (6) is reacted with n-BuLi in an ethyl alcohol solvent And then reacted with i (iso) -Pr-O-B (C6H12O2) to obtain a pale yellow solid compound (7) yield 84%. In the case of producing the compound shown by the formula (1), the compound (5) to the compound (7) can be replaced with each other so that the desired Y can be produced.

References:

YOKOHAMA NATIONAL UNIVERSITY;YOKOYAMA, YASUSHI;NAKAGAWA, TETSUYA;TAKEUCHI, SAKIKO JP2017/160159, 2017, A Location in patent:Paragraph 0045