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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Methylbenzimidazole → 2-Methyl-1-propyl-1H-benzimidazole

HRID 1970685
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HRID 1970685 반응식
[CH3:1][C:2]1[NH:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[H-].[Na+].I[CH2:14][CH2:15][CH3:16]>O1CCCC1>[CH3:1][C:2]1[N:6]([CH2:14][CH2:15][CH3:16])[C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N:3]=1
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참가 물질

5

반응물 3

HCID 119842-MethylbenzimidazoleHCID 24758Sodium hydrideHCID 336431-Iodopropane

생성물 1

HCID 7998002-Methyl-1-propyl-1H-benzimidazole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a flask were added 2.0 g 2-methylbenzimidazole and 40 ml tetrahydrofuran and the mixture was cooled to 10 C under nitrogen. 0.9 g Sodium hydride were added in portions and the reaction mixture was stirred for 20 minutes. 3.9 g 1-iodopropane were added and the mixture was heated to 45 C for 6 hours. The mixture was quenched slowly with 40 ml water, extracted twice with ethyl acetate and washed with water. Following solvent removal, the product was purified by silica gel chromatography using pure ethyl acetate to 5% methanol in ethyl acetate. A pale yellow oil was obtained.

후처리

  1. temperaturethe mixture was cooled to 10 C under nitrogen
  2. temperaturethe mixture was heated to 45 C for 6 hours
  3. customThe mixture was quenched slowly with 40 ml water
  4. extractionextracted twice with ethyl acetate
  5. washwashed with water
  6. customFollowing solvent removal
  7. customthe product was purified by silica gel chromatography
  8. customA pale yellow oil was obtained

출처 및 근거

ORD 기록
ord-c3a183dfbad9400eb21fe4896878885c
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431045B2

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