Hydrochloric Acid → (10-Phenylanthracen-9-yl)boronic acid

HRID 571589

反応式

HRID 571589 の反応式
Br[C:2]1[C:3]2[C:8]([C:9]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.C([Li])CCC.[B:27](OCC)([O:31]CC)[O:28]CC.Cl>C1COCC1.CCCCCC>[C:16]1([C:9]2[C:8]3[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=3)[C:2]([B:27]([OH:31])[OH:28])=[C:15]3[C:10]=2[CH:11]=[CH:12][CH:13]=[CH:14]3)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 9009Triethyl borateHCID 41558369-Bromo-10-phenyl-anthraceneHCID 178418339Butyllithium

生成物 1

HCID 22247164(10-Phenylanthracen-9-yl)boronic acid収率 80%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 8058Hexane溶媒

反応条件

温度
-80 °C

実験手順

An amount of 14 g (42 mmol) of 9-bromo-10-phenylanthracene was dissolved in dehydrated THF and cooled to −80° C. Then, 31.2 ml (49 mmol) of a solution of n-butyllithium in n-hexane was added dropwise. Forty minutes later, 13 g (89 mmol) of triethyl borate was added. After two-hour reaction, a diluted hydrochloric acid solution was added and allowed to stand for 12 hours. Then, the separated organic layer was recrystallized to obtain 10 g (33.6 mmol) of 10-phenylanthracene-9-boronic acid. The yield was 75.2%.

後処理

  1. customAfter two-hour reaction
  2. customThen, the separated organic layer was recrystallized

出典と根拠

ORDレコード
ord-53195f9b7d5c4567a407a4299eb76c23
出典データセット
uspto-grants-2015_05
特許番号
US09028976B2

関連ノート

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