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Methyl iodide → (4R)-4,5-Dihydro-2-(methylthio)-4-thiazolemethanol

HRID 1957376
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HRID 1957376 반응식
[OH:1][CH2:2][C@@H:3]1[CH2:7][S:6][C:5]([SH:8])=[N:4]1.[CH:9](N(C(C)C)CC)(C)C.CI>CO>[OH:1][CH2:2][C@@H:3]1[CH2:7][S:6][C:5]([S:8][CH3:9])=[N:4]1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 81531DiisopropylethylamineHCID 178521049HCID 178521049, 화합물2회

생성물 1

HCID 22862349(4R)-4,5-Dihydro-2-(methylthio)-4-thiazolemethanol수율 59%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture solution of 4.88 g of 4(R)-hydroxymethyl-2-mercapto-1,3-thiazoline [Compound (5)] and 22.8 ml of diisopropylethylamine in 65 ml of dry methanol was added 14.00 g of methyl iodide under refluxing condition, and the reaction mixture was refluxed for 1 hour. After removal of the solvent under reduced pressure, the resulting residue was dissolved in ethyl acetate and the organic layer was washed with saturated sodium bicarbonate solution, water and saturated saline solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the resulting residue was purified by silica gel column chromatography (chloroform-acetone) to give 3.14 g (59%) of 4(R)-hydroxymethyl-2-methylthio-1,3-thiazoline [Compound (6)].

후처리

  1. temperatureunder refluxing condition
  2. temperaturethe reaction mixture was refluxed for 1 hour
  3. customAfter removal of the solvent under reduced pressure
  4. dissolutionthe resulting residue was dissolved in ethyl acetate
  5. washthe organic layer was washed with saturated sodium bicarbonate solution, water and saturated saline solution
  6. dry with materialdried over magnesium sulfate
  7. customThe solvent was removed under reduced pressure
  8. customthe resulting residue was purified by silica gel column chromatography (chloroform-acetone)

출처 및 근거

ORD 기록
ord-060f4bd975894dc8a351c241cc99c3fa
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05783703

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