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Methyl iodide → HCID 86663637, 화합물

HRID 1777199
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HRID 1777199 반응식
[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[CH:8]([OH:12])[CH2:7][CH2:6][CH2:5][C:4]=2[N:3]=1.[H-].[Na+].[CH3:15]I>O1CCCC1>[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[CH:8]([O:12][CH3:15])[CH2:7][CH2:6][CH2:5][C:4]=2[N:3]=1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 44116687HCID 44116687, 화합물

생성물 1

HCID 86663637HCID 86663637, 화합물수율 61%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2-chloro-5,6,7,8-tetrahydroquinolin-5-ol (319 mg, 1.737 mmol) in tetrahydrofuran (8 mL) was added in small portions sodium hydride (83 mg, 2.085 mmol; 60 on mineral oil). After stirring the resulting suspension for 20 min at RT methyl iodide (0.119 ml, 1.911 mmol) was added dropwise. The reaction mixture was stirred at RT for 20 h. The reaction was quenched by addition of a saturated ammonium chloride solution. The layers were separated and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were washed with brine and dried over sodium sulfate, filtered, and evaporated to dryness. The crude was purified by flash chromatography (silica gel, cyclohexane/ethylacetate) yielding a slightly yellow oil. Amount 210 mg. Yield 61%.

후처리

  1. additionwas added dropwise
  2. customThe reaction was quenched by addition of a saturated ammonium chloride solution
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with ethyl acetate (3×)
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated to dryness
  9. customThe crude was purified by flash chromatography (silica gel, cyclohexane/ethylacetate)
  10. customyielding a slightly yellow oil

출처 및 근거

ORD 기록
ord-ef1b3f31014f4e66b9ae76ece6d1ffb8
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09266855B2

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