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

Hydrochloric Acid → 1-Methyl-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazole-4-carboxylic acid

HRID 1674484
노트
인쇄 미리보기

반응식

HRID 1674484 반응식
C([O:3][C:4]([CH:6]1[CH2:10][N:9]([CH3:11])[N:8]=[C:7]1[C:12]([F:15])([F:14])[F:13])=[O:5])C.[OH-].[Na+].Cl>O1CCOCC1>[CH3:11][N:9]1[CH2:10][CH:6]([C:4]([OH:5])=[O:3])[C:7]([C:12]([F:13])([F:14])[F:15])=[N:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 67339313HCID 67339313, 화합물

생성물 1

HCID 673400881-Methyl-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazole-4-carboxylic acid

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

1-Methyl-3-trifluoromethyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid ethyl ester (20 g, 90 mmol) was dissolved in 400 ml of dioxan. 400 ml of a 1 N aqueous sodium hydroxide solution (0.4 mol) were added and the reaction mixture was stirred for 2 h at room temperature. Subsequently the mixture was acidified with concentrated hydrochloric acid (pH 2). The dioxan was removed in vacuo, the residue was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over magnesium sulfate and evaporated, delivering 15 g of 1-methyl-3-trifluoromethyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid, which could be directly used in the next step without further purification.

후처리

  1. customThe dioxan was removed in vacuo
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. customcould be directly used in the next step without further purification

출처 및 근거

ORD 기록
ord-a327e625aeff4945842a4b7e3be99e29
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003626B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트