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Dimethylformamide → 3-[[8-([1,1'-Biphenyl]-4-yloxy]octyl]oxy]-2-methoxy-1-propanol

HRID 35949
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HRID 35949 반응식
[C:1]1([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[CH:6]=[CH:5][C:4]([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][CH2:17][CH:18](O)[CH2:19][O:20]C(C2C=CC(OC)=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:3][CH:2]=1.CCCCCC.CN(C)[CH:57]=[O:58]>O1CCCC1>[C:1]1([C:43]2[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=2)[CH:6]=[CH:5][C:4]([O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][CH2:17][CH:18]([O:58][CH3:57])[CH2:19][OH:20])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 8058HexaneHCID 19939569HCID 19939569, 화합물

생성물 1

HCID 677861083-[[8-([1,1'-Biphenyl]-4-yloxy]octyl]oxy]-2-methoxy-1-propanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 7.6 g of 1-[[8-([1,1'-biphenyl]-4-yloxy)octyl]oxy]-3-[(4-methoxyphenyl)diphenylmethoxy]-2-propanol in 20 ml of dimethylformamide and 20 ml of tetrahydrofuran was added dropwise to a solution of 849 mg of hexane washed 50% sodium hydride in 50 ml of dimethylformamide containing 5.02 g of methyl iodide over 35 minutes under argon. The mixture was stirred overnight then ice was cautiously added followed by 300 ml of iced water. This mixture was extracted three times with ether, the extracts combined, washed with water, dried and evaporated. The residue was taken up in 65 ml of chloroform and 130 ml of methanol, heated to boiling, 8 g of Amberlite® IR-4B ion exchange resin added, stirred for 2 hours, filtered and evaporated. The residue was purified by chromatography, giving 1.27 g of 3-[[8-([1,1'-biphenyl]-4-yloxy]octyl]oxy]-2-methoxy- 1-propanol.

후처리

  1. washwashed 50% sodium hydride in 50 ml of dimethylformamide containing 5.02 g of methyl iodide over 35 minutes under argon
  2. additionice was cautiously added
  3. extractionThis mixture was extracted three times with ether
  4. washwashed with water
  5. customdried
  6. customevaporated
  7. temperature130 ml of methanol, heated
  8. addition8 g of Amberlite® IR-4B ion exchange resin added
  9. stirringstirred for 2 hours
  10. filtrationfiltered
  11. customevaporated
  12. customThe residue was purified by chromatography

출처 및 근거

ORD 기록
ord-69cc414d883149e6adf38e0b512aaeec
출처 데이터셋
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05411983

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