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Hydrochloric Acid → (2-Hydroxyphenyl)boronic acid

HRID 54193
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HRID 54193 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[B:9](OC)([O:12]C)[O:10]C.Cl>C1COCC1>[OH:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[B:9]([OH:12])[OH:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 72442-BromophenolHCID 8470Trimethyl borate

생성물 1

HCID 2773454(2-Hydroxyphenyl)boronic acid수율 95.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

Part B: 2-Bromophenol (10.0 g, 57.8 mmol) was dissolved in dry THF (100 ml) in a dry 250 ml flask flushed with nitrogen. The mixture was chilled in a dry ice/2-propanol bath, n-butyl lithium (51 ml of a 2.5M solution in hexanes, 127.2 mmol) was added then the cooling bath was exchanged for an ice-water bath. The reaction was stirred for an hour at 0° C. then trimethyl borate (6.9 ml, 60.7 mmol) was added to the slurry which became homogeneous after a few minutes. The mixture was stirred at room temperature overnight then treated with 2N aqueous HCl to pH 3, mixed well for 30 minutes and extracted with ether (3×25 ml). The organic materials were combined, dried (MgSO4) then concentrated under reduced pressure which gave 7.6 g (91%) of 2-hydroxybenzeneboronic acid as a white solid, m.p. 156°-158° C.

후처리

  1. customflushed with nitrogen
  2. temperatureThe mixture was chilled in a dry ice/2-propanol bath
  3. additionn-butyl lithium (51 ml of a 2.5M solution in hexanes, 127.2 mmol) was added
  4. customthe cooling bath was exchanged for an ice-water bath
  5. waitbecame homogeneous after a few minutes
  6. stirringThe mixture was stirred at room temperature overnight
  7. additionmixed well for 30 minutes
  8. extractionextracted with ether (3×25 ml)
  9. dry with materialdried (MgSO4)
  10. concentrationthen concentrated under reduced pressure which

출처 및 근거

ORD 기록
ord-bcdddbe9ef544c1db1c4749dadfff855
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05622937

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