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

Hydrochloric Acid → (2E)-3-[6-(Trifluoromethyl)pyridin-3-yl]prop-2-enoic acid

HRID 1880611
노트
인쇄 미리보기

반응식

HRID 1880611 반응식
C([O:3][C:4](=[O:17])/[CH:5]=[CH:6]/[C:7]1[CH:8]=[N:9][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:11][CH:12]=1)C.[OH-].[Na+].Cl>C1COCC1.CCO>[F:15][C:13]([F:14])([F:16])[C:10]1[N:9]=[CH:8][C:7](/[CH:6]=[CH:5]/[C:4]([OH:17])=[O:3])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 59526503HCID 59526503, 화합물

생성물 1

HCID 5709645(2E)-3-[6-(Trifluoromethyl)pyridin-3-yl]prop-2-enoic acid수율 91.7%

시약·촉매·용매 1

HCID 21873804Tetrahydrofuran ethanol용매

실험 절차

To a solution of (E)-ethyl-3-(6-(trifluoromethyl)pyridin-3-yl)acrylate (2.65 g, 10.8 mmol) in THF/EtOH (1/1, 20 mL) was added 2.28 M NaOH (aq.) (14.2 mL) at rt. The reaction mixture was stirred at rt for 4 h and was then neutralized by adding 1M HCl(aq.). The water-phase was extracted with CH2Cl2/MeOH 9/1 (5×20 mL), the combined organics dried (MgSO4), filtered and evaporated to give the title compound (2.15 g, 9.90 mmol, 91%) as an off white solid. This material was used directly in the next step without further purification.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. extractionThe water-phase was extracted with CH2Cl2/MeOH 9/1 (5×20 mL)
  2. dry with materialthe combined organics dried (MgSO4)
  3. filtrationfiltered
  4. customevaporated

출처 및 근거

ORD 기록
ord-496c0e5c594c4f10be15ef074dae5a98
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318768B2

반응 노트

불러오는 중…