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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 86706919, 화합물

HRID 1772332
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HRID 1772332 반응식
[CH3:1][O:2][CH2:3][C@H:4]([OH:7])[CH2:5][OH:6].[S:8](Cl)(Cl)=[O:9].I([O-])(=O)(=O)=[O:13].[Na+].O>C(Cl)Cl.C(OCC)C.[Ru](Cl)(Cl)Cl>[CH3:1][O:2][CH2:3][C@H:4]1[CH2:5][O:6][S:8](=[O:9])(=[O:13])[O:7]1
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참가 물질

8

반응물 4

HCID 962WaterHCID 24386Thionyl ChlorideHCID 7014878(2R)-3-methoxypropane-1,2-diolHCID 23667635Sodium periodate

생성물 1

HCID 86706919HCID 86706919, 화합물

시약·촉매·용매 3

HCID 61850Ruthenium trichloride촉매
HCID 3283
Diethyl Ether
용매
HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

To a solution of crude (R)-3-methoxypropane-1,2-diol (7.66 g, 72.2 mmol) in DCM (100 mL) was slowly (˜10 min) added thionyl chloride (6.32 mL, 87 mmol) at rt. When the addition was completed, the dark brown solution was heated to reflux for 1 h before concentrating it to ˜10-20 mL under vacuum. Then, the cyclic sulfite was dissolved in DCM (80 mL) and acetonitrile (80 mL) and cooled to 0° C. Ruthenium(III) chloride (0.075 g, 0.361 mmol) and sodium periodate (23.16 g, 108 mmol) were added followed by water (100 mL). The biphasic reaction was vigorously stirred at 0° C. for 1 h. The reaction was finally diluted with diethyl ether (600 mL) and the product was sequentially washed with water, a saturated solution of sodium bicarbonate (repeated twice) and brine. The organic layer was dried over Na2SO4, filtered through a pad of silica gel (the pad was rinsed with diethyl ether) and concentrated under vacuum. The turbid liquid was used in the next step without purification.

후처리

  1. custom(˜10 min)
  2. additionWhen the addition
  3. temperaturethe dark brown solution was heated
  4. temperatureto reflux for 1 h
  5. concentrationbefore concentrating it to ˜10-20 mL under vacuum
  6. dissolutionThen, the cyclic sulfite was dissolved in DCM (80 mL)
  7. customThe biphasic reaction
  8. washthe product was sequentially washed with water
  9. dry with materialThe organic layer was dried over Na2SO4
  10. filtrationfiltered through a pad of silica gel (the pad
  11. washwas rinsed with diethyl ether) and
  12. concentrationconcentrated under vacuum
  13. customThe turbid liquid was used in the next step without purification

출처 및 근거

ORD 기록
ord-f248fbd67cc34d1ea29180df3ba11c18
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249161B2

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