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

HCID 58545553, 화합물 → HCID 58545574, 화합물

HRID 79935
노트
인쇄 미리보기

반응식

HRID 79935 반응식
CON(C)[C:4]([C:6]1[S:10][CH:9]2[CH:11]=[CH:12][S:13][CH:8]2[CH:7]=1)=[O:5].[CH3:15][Mg]Br>C1COCC1>[S:10]1[C:6]([C:4](=[O:5])[CH3:15])=[CH:7][CH:8]2[S:13][CH:12]=[CH:11][CH:9]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 58545553HCID 58545553, 화합물HCID 178418573HCID 178418573, 화합물

생성물 1

HCID 58545574HCID 58545574, 화합물수율 124.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

3a,6a-Dihydro-thieno[3,2-b]thiophene-2-carboxylic acid methoxy-methyl-amide (1.955 g, 8.60 mmol) was dissolved in THF. The stirred solution was cooled to 0° C. before methylmagnesium bromide (1.4 M in PhMe, 8.6 mL, 12.04 mmol) was added. The reaction was allowed to gradually warm to RT o/n, then it was quenched by addition of 10% HCl. The aqueous phase was extracted with diethyl ether. The organic phase was washed with brine then dried over MgSO4, filtered and concentrated to afford the title compound (1.98 g, 80%).

후처리

  1. additionwas added
  2. customwas quenched by addition of 10% HCl
  3. extractionThe aqueous phase was extracted with diethyl ether
  4. washThe organic phase was washed with brine
  5. dry with materialthen dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f8cb742975b341e38f03622fbe01745f
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841278B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트