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Water → HCID 86747712, 화합물

HRID 488160
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HRID 488160 반응식
[OH-].[Na+].[C:3]([S:6][CH2:7][P:8](=[O:15])([O:12][CH2:13][CH3:14])[O:9][CH2:10][CH3:11])(=O)[CH3:4].[CH3:16]/[C:17](/[CH2:22][CH2:23]/[CH:24]=[C:25](\[CH3:32])/[CH2:26][CH2:27][CH:28]=[C:29]([CH3:31])[CH3:30])=[CH:18]\CCI.O>C(O)C>[CH3:18]/[C:17](/[CH2:22][CH2:23]/[CH:24]=[C:25](\[CH3:32])/[CH2:26][CH2:27][CH:28]=[C:29]([CH3:31])[CH3:30])=[CH:16]\[CH2:4][CH2:3][S:6][CH2:7][P:8](=[O:15])([O:12][CH2:13][CH3:14])[O:9][CH2:10][CH3:11]
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HCID 962WaterHCID 14798Sodium Hydroxide2회HCID 10871691HCID 10871691, 화합물HCID 12536443S-[(Diethoxyphosphoryl)methyl] ethanethioate

생성물 1

HCID 86747712HCID 86747712, 화합물수율 94.2%

시약·촉매·용매 1

HCID 702Ethanol용매
2회

실험 절차

Solid sodium hydroxide (0.14 g, 3.5 mmol) was added to a stirred solution of diethyl acetylthiomethylphosphonate (0.59 g, 2.5 mmol) in ethanol (10 mL). The resulting mixture was stirred at room temperature under nitrogen until all the sodium hydroxide dissolved, then added a solution of (E,E)-4,8,12-trimethyl-3,7,11-tridecatrienyl iodide (0.84 g, 2.4 mmol) in ethanol (2 mL). The resulting mixture was stirred at room temperature under nitrogen overnight. The reaction mixture was poured into cold water and extracted with ether. The ethereal extract was washed with water, dried, filtered and evaporated to give a residue, which was purified by flash chromatography on a silica gel column. Elution of the column with methylene:acetate (10:1, v:v) afforded the title compound (0.91 g, 2.26 mmol, 94%) as a colorless oil.

후처리

  1. dissolutiondissolved
  2. extractionextracted with ether
  3. extractionThe ethereal extract
  4. washwas washed with water
  5. customdried
  6. filtrationfiltered
  7. customevaporated
  8. customto give a residue, which
  9. customwas purified by flash chromatography on a silica gel column
  10. washElution of the column with methylene:acetate (10:1, v:v)

출처 및 근거

ORD 기록
ord-48ad5355942b4ae89c976f228591e9bf
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05298655

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