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

Ethyl Acetate → Tert-butyl 6-bromo-2H-chromene-3-carboxylate

HRID 1277187
노트
인쇄 미리보기

반응식

HRID 1277187 반응식
[Br:1][C:2]1[CH:9]=[C:6]([CH:7]=O)[C:5]([OH:10])=[CH:4][CH:3]=1.[C:11]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])(=[O:14])[CH:12]=[CH2:13].CC(C)([O-])C.[K+].C(OCC)(=O)C>C(O)(C)(C)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:13][C:12]([C:11]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[CH:7][C:6]=2[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 15458tert-Butyl acrylateHCID 728635-BromosalicylaldehydeHCID 23665647Potassium tert-butoxide

생성물 1

HCID 10566979Tert-butyl 6-bromo-2H-chromene-3-carboxylate

시약·촉매·용매 1

HCID 6386tert-Butanol용매

실험 절차

To a solution of 5-bromosalicylaldehyde (10.0 g) and tert-butyl acrylate (17.5 ml) in tert-butanol (100 ml) was added potassium tert-butoxide (1.67 g) at room temperature, and the mixture was refluxed for 66 hours and cooled to room temperature. To the mixture was added ethyl acetate, and the mixture was washed with water, 1N sodium hydroxide and saturated sodium chloride solution, dried with magnesium sulfate and concentrated. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:19) to give tert-butyl 6-bromo-2H-1-benzopyran-3-carboxylate (10.86 g) as pale yellow crystals.

후처리

  1. temperaturethe mixture was refluxed for 66 hours
  2. washthe mixture was washed with water, 1N sodium hydroxide and saturated sodium chloride solution
  3. dry with materialdried with magnesium sulfate
  4. concentrationconcentrated
  5. customThe residue was separated
  6. custompurified with column chromatography (ethyl acetate/hexane=1:19)

출처 및 근거

ORD 기록
ord-54ca61cd09a74cc0a9f5734447714415
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06166006

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트