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Benzene, 1-iodo-2-(trifluoromethyl)- → HCID 94776684, 화합물

HRID 1771416
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HRID 1771416 반응식
I[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([F:11])([F:10])[F:9].[Li]CCCC.[O:17]1[C@H:19]([CH2:20][CH3:21])[CH2:18]1>C1COCC1>[F:9][C:8]([F:11])([F:10])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[CH2:18][C@H:19]([OH:17])[CH2:20][CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 67957Benzene, 1-iodo-2-(trifluoromethyl)-HCID 11147670(2R)-2-EthyloxiraneHCID 178418339Butyllithium

생성물 1

HCID 94776684HCID 94776684, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

2-Iodobenzotrifluoride (3 g) was dissolved in THF (18 ml) and was cooled to −78° C. n-BuLi (2.5 M in hexanes, 13.23 ml) was added dropwise to the reaction mixture. After 1 h, (R)-(+)-1,2-epoxybutane (1.4 ml) in THF (18 ml) was added. The reaction temperature was slowly increased to rt. The mixture was poured into ice-water (100 ml), and the product was extracted with heptane. The organic phase was washed with brine and water, dried (Na2SO4) ja evaporated under vacuum. The title compound was obtained by separation method E. (Yield 1.05 g).

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후처리

  1. additionwas added dropwise to the reaction mixture
  2. extractionthe product was extracted with heptane
  3. washThe organic phase was washed with brine and water
  4. dry with materialdried (Na2SO4) ja
  5. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-b5a09e078b65404083ccd2f657daf21b
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249127B2

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