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

Triethylsilane → HCID 18545868, 화합물

HRID 275710
노트
인쇄 미리보기

반응식

HRID 275710 반응식
[CH3:1][C:2]1[C:7]2[CH:8]([C:12]([OH:14])=[O:13])[CH2:9][C:10](=O)[C:6]=2[CH:5]=[CH:4][CH:3]=1.C([SiH](CC)CC)C>FC(F)(F)C(O)=O>[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:7]=1[CH:8]([C:12]([OH:14])=[O:13])[CH2:9][CH2:10]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12052TriethylsilaneHCID 2895327-Methyl-3-oxo-2,3-dihydro-1h-indene-1-carboxylic acid

생성물 1

HCID 18545868HCID 18545868, 화합물수율 82.7%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

To a solution of 12a (100 g) in trifluoroacetic acid is added trietylsilane (141 g). The mixture was stirred for 72 hours at room temperature and was then evaporated in vacuo the residue was dissolved in ethyl acetate and was extracted with dilute NaOH solution. The aqueous phase was washed with etyl acetate and was then acidified with concentrated hydrochloric acid. Conventional work up with ethyl acetate gave 80.4 g of crude product. Purification on silica gel eluted with ethyl acetate-heptane-acetic acid gave the title compound (76.6 g).

후처리

  1. customwas then evaporated in vacuo the residue
  2. dissolutionwas dissolved in ethyl acetate
  3. extractionwas extracted with dilute NaOH solution
  4. washThe aqueous phase was washed with etyl acetate
  5. customgave 80.4 g of crude product
  6. customPurification on silica gel
  7. washeluted with ethyl acetate-heptane-acetic acid

출처 및 근거

ORD 기록
ord-3086b06997da4e0799f585676bc84d58
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06352988B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트