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Hydrochloric Acid → 4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)

HRID 909961
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HRID 909961 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.CCCCCC.C([Li])CCC.[B:29](OC(C)C)([O:34]C(C)C)[O:30]C(C)C.Cl>C1(C)C=CC=CC=1.C1COCC1>[C:8]1([C:5]2[CH:6]=[CH:7][C:2]([B:29]([OH:34])[OH:30])=[CH:3][CH:4]=2)[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=1
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참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 8058HexaneHCID 21531Triisopropyl borateHCID 112083381-(4-Bromophenyl)naphthaleneHCID 178418339Butyllithium

생성물 1

HCID 441193994-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)수율 68.9%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 8028Tetrahydrofuran용매

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온도
-60 °C

실험 절차

Under an argon gas atmosphere, a mixture of 208.8 g (737.4 mmol) of 1(4-bromophenyl)naphthalene and 2.1 L of dehydrated THF was cooled down to −60 degrees C., and added with 567 ml (884.9 mmol) of hexane solution of 1.56M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for two hours at −60 degree C. 416 g (2.21 mol) of triisopropyl borate was dropped into the reaction solution at −60 degrees C. Subsequently, the reaction mixture was stirred for 17 hours at room temperature. The reaction mixture was further added with solution of hydrochloric acid to be stirred for one hour at room temperature. After the reaction, the reaction mixture was further added with toluene, so that aqueous phase thereof was eliminated. After organic phase thereof was dried with magnesium sulfate, the solvent was distilled away under reduced pressure. By recrystallizing the obtained solid by toluene, 126 g of 4-(1-naphthyl)phenylboronic acid was obtained at an yield of 67%.

후처리

  1. stirringThen, the reaction mixture was stirred for two hours at −60 degree C
  2. stirringSubsequently, the reaction mixture was stirred for 17 hours at room temperature
  3. stirringto be stirred for one hour at room temperature
  4. customAfter the reaction
  5. dry with materialAfter organic phase thereof was dried with magnesium sulfate
  6. distillationthe solvent was distilled away under reduced pressure
  7. customBy recrystallizing the obtained solid by toluene

출처 및 근거

ORD 기록
ord-d3108a549e304c4ba1a76dfe8e26712a
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08021574B2

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