홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Tetrahydrofuran → (2-Methyl-1H-benzimidazol-4-yl)methanol

HRID 1723110
노트
인쇄 미리보기

반응식

HRID 1723110 반응식
[CH3:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([C:11](OCC)=[O:12])[C:4]=2[N:3]=1.O1CCCC1.[AlH4-].[Li+].C(OCC)(=O)C>O>[CH3:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([CH2:11][OH:12])[C:4]=2[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8028Tetrahydrofuran2회HCID 8857Ethyl AcetateHCID 28112Lithium aluminum hydrideHCID 18680979ethyl 2-methyl-1H-benzimidazole-4-carboxylate

생성물 1

HCID 20026664(2-Methyl-1H-benzimidazol-4-yl)methanol수율 79.4%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

(a-2) A cooled (0° C.) solution of 10 parts of ethyl 2-methyl-1H-benzimidazole-4-carboxylate in 45 parts of tetrahydrofuran was added dropwise to a suspension of 4 parts of lithium tetrahydroaluminate in 45 parts of tetrahydrofuran. Upon complete addition, the temperature was allowed to reach room temperature. After the addition of ethyl acetate and water, the reaction mixture was filtered over diatomaceous earth. The filtrate was evaporated, yielding 6.3 parts (79.4%) of 2-methyl-1H-benzimidazole-4-methanol as a residue (int. 66).

후처리

  1. additionUpon complete addition
  2. customto reach room temperature
  3. filtrationthe reaction mixture was filtered over diatomaceous earth
  4. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-fdcb98520d294504a9287656ca2d82b5
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04859684

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트