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

Methyl iodide → 2-Methyl-1,2,4,5-tetrahydro-benzo[c]azepin-3-one

HRID 1688108
노트
인쇄 미리보기

반응식

HRID 1688108 반응식
[H-].[Na+].[CH2:3]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH2:7][CH2:6][C:5](=[O:14])[NH:4]1.[CH3:15]I>C1COCC1>[CH3:15][N:4]1[C:5](=[O:14])[CH2:6][CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 28330792,3,4,5-tetrahydro-1H-2-benzazepin-3-one

생성물 1

HCID 109100902-Methyl-1,2,4,5-tetrahydro-benzo[c]azepin-3-one수율 95%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

At 25° C., sodium hydride (150 mg, 6.3 mmol) was added to a solution of 1,2,4,5-tetrahydro-benzo[c]azepin-3-one (1 g, 6 mmol) in THF (50 mL). The suspension was stirred for 10 minutes and treated with methyl iodide (1 g, 7 mmol). The mixture was stirred for an additional 4 hours and then partitioned between ethyl acetate (100 ml) and water (50 ml). Washing once with brine (30 ml), drying over anhydrous magnesium sulfate and evaporation of solvent gave 2-methyl-1,2,4,5-tetrahydro-benzo[c]azepin-3-one (1 g, 5.7 mmol, 95%): 1H NMR (300 MHz, CDCl3) δ 7.2 (m, 5H), 4.52 (s, 2H), 3.18 (t, 2H), 3.09 (s, 3H), 3.00 (t, 2H).

후처리

  1. stirringThe mixture was stirred for an additional 4 hours
  2. custompartitioned between ethyl acetate (100 ml) and water (50 ml)
  3. washWashing once with brine (30 ml)
  4. dry with materialdrying over anhydrous magnesium sulfate and evaporation of solvent

출처 및 근거

ORD 기록
ord-abaaa25dc92648a1905c77cb55c6e13e
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148391B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트