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Boron tribromide → HCID 13493842, 화합물

HRID 414075
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HRID 414075 반응식
[CH2:1]([N:3]1[CH2:7][CH2:6][CH2:5][CH:4]1[CH2:8][NH:9][C:10](=[O:24])[C:11]1[C:16]([O:17][CH2:18][CH3:19])=[CH:15][CH:14]=[C:13]([Br:20])[C:12]=1[O:21]CC)[CH3:2].B(Br)(Br)Br>C(Cl)Cl>[CH2:1]([N:3]1[CH2:7][CH2:6][CH2:5][CH:4]1[CH2:8][NH:9][C:10](=[O:24])[C:11]1[C:16]([O:17][CH2:18][CH3:19])=[CH:15][CH:14]=[C:13]([Br:20])[C:12]=1[OH:21])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 15565720HCID 15565720, 화합물

생성물 1

HCID 13493842HCID 13493842, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

10.0 g (0.023 mole) of (-)-N-ethyl-2-(3-bromo-2,6-diethoxybenzamidomethyl)pyrrolidine is dissolved in 250 ml of methylene chloride. 2.4 ml (0.025 mole) of boron tribromide is added. The mixture is left over night at room temperature and is then washed with 2N NH3. The extract is dried with Na2SO4 and evaporated. The oily residue crystallizes after a while. Petroleum ether is added to the product, which is then filtered off. Yield 7.0 g. M.p. 74°-76° C. [α]D20 =-66.7° (1% acetone).

후처리

  1. waitThe mixture is left over night at room temperature
  2. washis then washed with 2N NH3
  3. dry with materialThe extract is dried with Na2SO4
  4. customevaporated
  5. customThe oily residue crystallizes after a while
  6. additionPetroleum ether is added to the product, which
  7. filtrationis then filtered off
  8. customM.p. 74°-76° C. [α]D20 =-66.7° (1% acetone)

출처 및 근거

ORD 기록
ord-92da08ccdfe748b9833b9742c746cfdc
출처 데이터셋
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04789683

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