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Trimethyl borate → Boronic acid, (4-ethylphenyl)-

HRID 232750
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HRID 232750 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH3:9])=[CH:4][CH:3]=1.[Mg].[B:11](OC)([O:14]C)[O:12]C>CCOCC>[CH2:8]([C:5]1[CH:6]=[CH:7][C:2]([B:11]([OH:14])[OH:12])=[CH:3][CH:4]=1)[CH3:9]
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참가 물질

5

반응물 3

HCID 8470Trimethyl borateHCID 153131-Bromo-4-ethylbenzeneHCID 5462224Magnesium2회

생성물 1

HCID 2734352Boronic acid, (4-ethylphenyl)-수율 41%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

실험 절차

A solution of 1-bromo-4-ethyl benzene (2.0 g, 11 mmol) in dry ether (5 ml) was added to magnesium turnings (311 mg, 13 mmol), which had been suspended in dry ether, by a dropwise addition. After addition was complete, the suspension was refluxed for a period of 15 min after which nearly all of the magnesium had reacted. This solution was then added to trimethy borate (1.12 g, 11 mmol) previously dissolved in ether (5 ml) at -78° C., the solution was warmed to room temperature and stirred for 90 min. The reaction was quenched by the addition of 10% aqueous HCl (2 ml) and the solution was extracted with ether. The combined ether extracts was extracted with 1M NaOH (2×20 ml), the aqueous extracts were acidified with dilute HCl to pH 2 and extracted with ether (2×25 ml). The combined ether extracts was washed once with water (10 ml), dried and evaporated to produce a white solid (676 mg, 38% yield), m.p. 138°-140° C.

후처리

  1. additionAfter addition
  2. customhad reacted
  3. customThe reaction was quenched by the addition of 10% aqueous HCl (2 ml)
  4. extractionthe solution was extracted with ether
  5. extractionThe combined ether extracts was extracted with 1M NaOH (2×20 ml)
  6. extractionextracted with ether (2×25 ml)
  7. washThe combined ether extracts was washed once with water (10 ml)
  8. customdried
  9. customevaporated

출처 및 근거

ORD 기록
ord-c1c147a2cbeb4858ba5715228f5b065a
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05591761

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