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Boron tribromide → HCID 9859510, 화합물

HRID 1167613
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HRID 1167613 반응식
C[O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:11][CH2:10][CH2:9][N:8]([CH2:12][CH2:13][NH:14][C:15](=[O:17])[CH3:16])[C:7]=2[CH:18]=1.B(Br)(Br)Br.C(=O)([O-])O.[Na+]>ClCCl>[OH:2][C:3]1[CH:4]=[CH:5][C:6]2[O:11][CH2:10][CH2:9][N:8]([CH2:12][CH2:13][NH:14][C:15](=[O:17])[CH3:16])[C:7]=2[CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 9859781HCID 9859781, 화합물

생성물 1

HCID 9859510HCID 9859510, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

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온도
-78 °C

실험 절차

Under argon, the compound obtained in Example 1 (342 mg; 1.37 mmol) is dissolved in 8 ml of distilled dichloromethane. The solution is cooled to −78° C., and then boron tribromide (4 eq.; 5.47 mmol; 5.17 μl) diluted with 5 ml of dichloromethane is slowly added. The mixture is left for one hour at −78° C. and then for 2 hours at ambient temperature. The reaction mixture is hydrolysed to pH 7 with a saturated sodium hydrogen carbonate solution and then the aqueous phase is extracted 4 times with dichloromethane. The organic phases are combined, and then removed under reduced pressure. The solid obtained is dissolved in a minimum amount of dichloromethane, precipitated in the presence of pentane, filtered, and then washed with an Et2O/pentane mixture.

후처리

  1. additionis slowly added
  2. waitfor 2 hours at ambient temperature
  3. extractionthe aqueous phase is extracted 4 times with dichloromethane
  4. customremoved under reduced pressure
  5. customThe solid obtained
  6. customprecipitated in the presence of pentane
  7. filtrationfiltered
  8. washwashed with an Et2O/pentane mixture

출처 및 근거

ORD 기록
ord-4e4487b04ed4426b9dfd75a1f39fcce2
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06620809B2

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