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

Trifluoroacetic acid → tert-butyl 4,5-dihydro-1H-pyrazole-5-carboxylate

HRID 1396848
노트
인쇄 미리보기

반응식

HRID 1396848 반응식
[C:1]([O:5][C:6]([CH3:9])([CH3:8])[CH3:7])(=[O:4])[CH:2]=[CH2:3].[Si]([CH:14]=[N+:15]=[N-:16])(C)(C)C.C(O)(C(F)(F)F)=O>C1(C)C=CC=CC=1.C(Cl)Cl>[NH:16]1[CH:2]([C:1]([O:5][C:6]([CH3:9])([CH3:8])[CH3:7])=[O:4])[CH2:3][CH:14]=[N:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6422Trifluoroacetic acidHCID 15458tert-Butyl acrylateHCID 167693Trimethylsilyldiazomethane

생성물 1

HCID 86706338tert-butyl 4,5-dihydro-1H-pyrazole-5-carboxylate수율 41.1%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6344Dichloromethane
용매

실험 절차

To a solution of t-butyl acrylate (17 g, 133 mmol) dissolved in toluene (200 mL) and n-hexanes (200 mL) was added TMS-diazomethane (99 mL, 199 mmol) over 10 minutes. After 1 h the reaction mixture was concentrated and the residue diluted with DCM (300 mL) and TFA (20.44 mL, 265 mmol) was added slowly over 15 minutes. After 30 minutes the reaction mixture was concentrated, basified with 1N NaOH and extracted into DCM (400 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, concentrated, and purified by filtration through a pad of silica gel eluting the product with 50% ethyl acetate/hexanes to afford 10 g (54.6 mmol) of 1,1-dimethylethyl 4,5-dihydro-1H-pyrazole-5-carboxylate as a yellow oil. LC-MS (ES) m/e 170.91 (M+H)+.

후처리

  1. concentrationAfter 1 h the reaction mixture was concentrated
  2. additionwas added slowly over 15 minutes
  3. concentrationAfter 30 minutes the reaction mixture was concentrated
  4. extractionextracted into DCM (400 mL)
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. filtrationpurified by filtration through a pad of silica gel eluting the product with 50% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-04d1c429c73e47e58e9c536121bef4ce
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901119B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트