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Trimethyl borate → HCID 90198540, 화합물

HRID 1748935
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HRID 1748935 반응식
[C:1]1([C:7]2[CH:19]=[CH:18][C:10]3[S:11][C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=4[C:9]=3[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([Li])CCC.C[O:26][B:27](OC)[O:28]C>O1CCCC1>[C:1]1([C:7]2[CH:19]=[CH:18][C:10]3[S:11][C:12]4[C:17]([B:27]([OH:28])[OH:26])=[CH:16][CH:15]=[CH:14][C:13]=4[C:9]=3[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8470Trimethyl borateHCID 135272452-Phenyldibenzo[b,d]thiopheneHCID 178418339Butyllithium

생성물 1

HCID 90198540HCID 90198540, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

2-bromo-dibenzo[b,d]thiophene (10 g), phenylboronic acid (5.1 g) tetrakis(triphenylphosphine)palladium (2.2 g) and potassium carbonate (18.38 g) were refluxed in a mixture of toluene (110 mL), ethanol (20 mL) and water (90 mL) overnight. The reaction was quenched with water and the toluene layer was removed and passed through a celite column and the toluene layer was evaporated in a rotary evaporator to yield 5.2 g 2-phenyl-dibenzo[b,d]thiophene. 2-phenyldibenzo[b,d]thiophene (5.2 g) was dissolved in anhydrous tetrahydrofuran (50 mL) under nitrogen atmosphere, and the solution was then cooled to −78° C. 20.0 mL of n-butyl lithium (1.6 M solution) was added dropwise into the reaction mixture, and continuously stirred to equilibriate to room temperature. The reaction mixture was then cool to −60° C., and trimethyborate (5.67 mL) was added and the reaction was allowed to stir overnight. The reaction was then quenched with 20% aqueous hydrochloric acid, and extracted the organic layer with ethyl acetate; ethyl acetate layer was then washed thoroughly with water and dried over anhydrous sodium sulfate, and was evaporated to dryness to yield 4.2 g of 8-phenyldibenzo[b,d]thiophene-4-boronic acid.

후처리

  1. customto equilibriate to room temperature
  2. temperatureThe reaction mixture was then cool to −60° C.
  3. stirringto stir overnight
  4. customThe reaction was then quenched with 20% aqueous hydrochloric acid
  5. extractionextracted the organic layer with ethyl acetate
  6. washethyl acetate layer was then washed thoroughly with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. customwas evaporated to dryness

출처 및 근거

ORD 기록
ord-8c4d668435204bb89871565690e9aebe
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09153787B2

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