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

Acetic Acid → HCID 9859076, 화합물

HRID 1045652
노트
인쇄 미리보기

반응식

HRID 1045652 반응식
[C:1]1(=[O:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]1=[N:11]O.[C:14](O)(=[O:16])[CH3:15]>C(OC(=O)C)(=O)C.[Zn]>[O:13]=[C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH:2]1[NH:11][C:14](=[O:16])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 6813148HCID 6813148, 화합물

생성물 1

HCID 9859076HCID 9859076, 화합물수율 66%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 7918Acetic Anhydride용매

실험 절차

Zinc powder (24 g, 367 mmol) was added to a solution of 3,4-dihydro-[1,2]naphthoquinone 2-oxime (21.5 g, 123 mmol) in acetic acid (200 mw) and acetic anhydride (150 ml), and the solution was stirred at room temperature for 12 hours. After filtration and removal of the solvents under reduced pressure, the residue was partitioned between water and chloroform. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was washed with ethyl acetate and dried to afford N-(1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)-acetamide (16.5 g, 81 mmol, 66%) as brown crystals.

후처리

  1. filtrationAfter filtration and removal of the solvents under reduced pressure
  2. customthe residue was partitioned between water and chloroform
  3. washThe organic layer was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customAfter removal of the solvent
  6. washthe residue was washed with ethyl acetate
  7. customdried

출처 및 근거

ORD 기록
ord-14810c1b78c149e2ad3146ee4c605435
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08569294B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트