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Boron trifluoride etherate → HCID 24771803, 화합물

HRID 2221429
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HRID 2221429 반응식
[CH3:1][C:2]1([CH3:16])[C:6]([CH3:7])=[CH:5][CH2:4][CH:3]1[C:8]1[CH2:15][CH2:14][C:11]2([O:13][CH2:12]2)[CH2:10][CH:9]=1.B(F)(F)F.CCOCC>C1(C)C=CC=CC=1>[CH3:1][C:2]1([CH3:16])[C:6]([CH3:7])=[CH:5][CH2:4][CH:3]1[C:8]1[CH2:15][CH2:14][CH:11]([CH:12]=[O:13])[CH2:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8000Boron trifluoride etherateHCID 24771795HCID 24771795, 화합물

생성물 1

HCID 24771803HCID 24771803, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

6-(2,2,3-Trimethyl-cyclopent-3-enyl)-1-oxa-spiro[2.5]oct-5-ene (XIV, 2.72 g, 12.5 mmol,), dissolved in toluene (5 ml), are added dropwise to a solution of BF3.OEt2 (1.7 ml) in toluene (20 ml). After 2 hours, the reaction solution is poured onto ice (10 ml), then the phases are separated and the organic phase is washed once with saturated NaCl solution. The organic phase is then dried over Na2SO4, filtered off and concentrated in a rotary evaporator. 2.07 g of crude product having a purity of 83% are obtained, which is used in the next step without being purified further.

후처리

  1. additionthe reaction solution is poured onto ice (10 ml)
  2. customthe phases are separated
  3. washthe organic phase is washed once with saturated NaCl solution
  4. dry with materialThe organic phase is then dried over Na2SO4
  5. filtrationfiltered off
  6. concentrationconcentrated in a rotary evaporator
  7. customare obtained
  8. customwithout being purified further

출처 및 근거

ORD 기록
ord-a1da55a08e7b431a94ec83c6969e9544
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07368613B2

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