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

HCID 10755030, 화합물 → HCID 10736209, 화합물

HRID 1532039
노트
인쇄 미리보기

반응식

HRID 1532039 반응식
Br[CH2:2][C:3]1[C:4]([O:13][CH2:14][CH3:15])=[N:5][O:6][C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9].[C:16]1(=[O:26])[NH:20][C:19](=[O:21])[C:18]2=[CH:22][CH:23]=[CH:24][CH:25]=[C:17]12.[K]>CN(C=O)C>[CH2:14]([O:13][C:4]1[C:3]([CH2:2][N:20]2[C:19](=[O:21])[C:18]3=[CH:22][CH:23]=[CH:24][CH:25]=[C:17]3[C:16]2=[O:26])=[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[O:6][N:5]=1)[CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10755030HCID 10755030, 화합물HCID 24194345Phthalimide potassium salt

생성물 1

HCID 10736209HCID 10736209, 화합물수율 60%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

반응 조건

온도
90 °C

실험 절차

A solusion of ethyl 4-bromomethyl-3-ethoxyisoxazole-5-carboxylate (5 g, 17.9 mmol) in DMF (85 mL) was added to a suspension of potassium phthalimid (3.6 g, 19,7 mmol) in DMF (125 mL) at 90° C. The resulting mixture was stirred at 90° C. for 40 min, then cooled and concentrated in vacuo. Water (250 mL) was added and the aqueous phase was extracted with diethylether (2×200 mL). The organic extracts were dried (MgSO4) and concentrated in vacuo to give a crude product which was recrystallized (EtOH) to yield the title compound (3.70 g, 60%): mp 93-94° C.

후처리

  1. temperaturecooled
  2. concentrationconcentrated in vacuo
  3. additionWater (250 mL) was added
  4. extractionthe aqueous phase was extracted with diethylether (2×200 mL)
  5. dry with materialThe organic extracts were dried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customto give a crude product which
  8. customwas recrystallized (EtOH)

출처 및 근거

ORD 기록
ord-2b604fe4f5eb44da989aea4a05c50954
출처 데이터셋
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06200999B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트