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

Methanol → 3,3,3-Trifluoro-2-oxopropanoic acid

HRID 1466734
노트
인쇄 미리보기

반응식

HRID 1466734 반응식
[F:1][C:2]([F:11])([F:10])[C:3](=[O:9])[C:4]([O:6]CC)=[O:5].[OH-].[Na+].CO>C(O)C.O>[F:1][C:2]([F:11])([F:10])[C:3](=[O:9])[C:4]([OH:6])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 2737239Ethyl 3,3,3-trifluoro-2-oxopropanoate

생성물 1

HCID 51777643,3,3-Trifluoro-2-oxopropanoic acid수율 99%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of ethyl 3,3,3-trifluoro-2-oxopropanoate (5 g, 29.36 mmol) in ethanol (30 ml) was slowly added aqueous sodium hydroxide ((2.35 g, 58.72 mmol, dissolved in water (30 ml)), and stirred for 20 h at room temperature until the starting material was consumed. The reaction mixture was concentrated and the resulting white solid was dissolved in water (100 ml). The aqueous layer was extracted by ethyl acetate (50 ml×2), and then the aqueous layer was adjusted PH to 1˜2 with concentrated HCl, and concentrated to give a white solid. The solid was added to methanol (200 ml) and stirred for overnight, filtered, and the filtrate was concentrated and dried to give the crude product (4.13 g, 99%) as a white solid, used in next step without further purification.

후처리

  1. customwas consumed
  2. concentrationThe reaction mixture was concentrated
  3. dissolutionthe resulting white solid was dissolved in water (100 ml)
  4. extractionThe aqueous layer was extracted by ethyl acetate (50 ml×2)
  5. concentrationconcentrated
  6. customto give a white solid
  7. stirringstirred for overnight
  8. filtrationfiltered
  9. concentrationthe filtrate was concentrated
  10. customdried

출처 및 근거

ORD 기록
ord-27f5700531104a47b23d5f85784dd2b2
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999985B2

반응 노트

불러오는 중…