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

Acetone → {(2R,3S)-3-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-4-oxoazetidin-2-yl}acetic acid

HRID 851418
노트
인쇄 미리보기

반응식

HRID 851418 반응식
[CH3:1][C:2]([C@@H:18]1[C@@H:21]([CH2:22]C=C)[N:20](C(=C(C)C)C(OC)=O)[C:19]1=[O:33])([O:4][C:5]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][CH:10]=1)=[O:6])[CH3:3].P([O-])([O-])([O-])=O.I([O-])(=O)(=O)=O.[Na+].[Mn]([O-])(=O)(=O)=[O:46].[K+].C[C:52](C)=[O:53]>O.O.CC(C)=O>[CH3:3][C:2]([C@H:18]1[C:19](=[O:33])[NH:20][C@@H:21]1[CH2:22][C:52]([OH:53])=[O:46])([O:4][C:5]([O:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]([N+:15]([O-:17])=[O:16])=[CH:13][CH:14]=1)=[O:6])[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 180AcetoneHCID 1061PhosphateHCID 516875Potassium PermanganateHCID 23667635Sodium periodate2회HCID 56623914methyl 2-{(3S,4R)-3-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-2-oxo-4-allylazetidin-1-yl}-3-methylbut-2-enoate

생성물 1

HCID 56618986
{(2R,3S)-3-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-4-oxoazetidin-2-yl}acetic acid

시약·촉매·용매 2

HCID 962Water용매HCID 18366337Propan-2-one--water (1/1)용매

실험 절차

To a solution of methyl 2-{(3S,4R)-3-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-2-oxo-4-allylazetidin-1-yl}-3-methylbut-2-enoate (72.9 mg) in acetone (2.03 ml) was added a 0.7 M solution of phosphate buffer (pH 6.8, 1.35 ml) at ambient temperature. To the resulting suspension was added dropwise a solution of sodium periodate (86.0 mg) in water (0.594 ml) at ambient temperature. After stirring for 10 minutes, the reaction mixture was added with sodium periodate (117.2 mg) and potassium permanganate (37.5 mg) and stirred at ambient temperature overnight. The resulting mixture was diluted with water-acetone (15 ml-15 ml) and filtered with celite and the filter cake was washed with water-acetone (1:1). The combined filtrates were concentrated in vacuo at 0° C., acidified to pH 1 with 10% aqueous phosphoric acid, and extracted with chloroform. The organic layer was extracted with chilled 10% aqueous sodium bicarbonate (X3). The aqueous extracts were acidified with 3 N hydrochloric acid and reextracted with chloroform (X3). The chloroform extracts were washed with saturated aqueous sodium chloride containing a small amount of 3 N hydrochloric acid, dried over magnesium sulfate, filtered, and evaporated to give {(2R,3S)-3-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-4-oxoazetidin-2-yl}acetic acid (36.4 mg) as an amorphous solid.

후처리

  1. stirringstirred at ambient temperature overnight
  2. filtrationfiltered with celite
  3. washthe filter cake was washed with water-acetone (1:1)
  4. concentrationThe combined filtrates were concentrated in vacuo at 0° C.
  5. extractionextracted with chloroform
  6. extractionThe organic layer was extracted
  7. temperaturewith chilled 10% aqueous sodium bicarbonate (X3)
  8. washThe chloroform extracts were washed with saturated aqueous sodium chloride containing a small amount of 3 N hydrochloric acid
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. customevaporated

출처 및 근거

ORD 기록
ord-56a4d762c7fe46b0846fb6d55c51fdb4
출처 데이터셋
uspto-grants-1983_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04383945

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트