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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 6-Methyl-2-methylaminobenzyl alcohol

HRID 1762184
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HRID 1762184 반응식
[CH:1]([NH:3][C:4]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[C:5]=1[CH2:6][OH:7])=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1>[CH3:12][C:8]1[C:5]([CH2:6][OH:7])=[C:4]([NH:3][CH3:1])[CH:11]=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 143684522-Formamido-6-methylbenzyl alcoholHCID 21226445Aluminium lithium hydride

생성물 1

HCID 540947806-Methyl-2-methylaminobenzyl alcohol수율 49.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2-formamido-6-methylbenzyl alcohol (1.9 g) in tetrahydrofuran (26 ml) was added dropwise to a suspension of lithium aluminum hydride (0.873 g) in tetrahydrofuran (17 ml) at room temperature over a period of 10 minutes. After being refluxed for 4.5 hours, the excess reagent was decomposed with a small amount of water and the resulting precipitates were filtered off by suction. The filtrate was evaporated in vacuo and the residue was recrystallized from carbon tetrachloride to give 6-methyl-2-methylaminobenzyl alcohol (0.86 g).

후처리

  1. temperatureAfter being refluxed for 4.5 hours
  2. customthe resulting precipitates
  3. filtrationwere filtered off by suction
  4. customThe filtrate was evaporated in vacuo
  5. customthe residue was recrystallized from carbon tetrachloride

출처 및 근거

ORD 기록
ord-d1b51f6357394f49aaea3d7e4e62f200
출처 데이터셋
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04831041

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