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

Formaldehyde → 2-Ethylacrylic Acid (ethyl 2-ethylacrylate)

HRID 80294
노트
인쇄 미리보기

반응식

HRID 80294 반응식
[C:1]([CH:6]([CH2:10][CH3:11])[C:7]([OH:9])=[O:8])([O:3]CC)=[O:2].C(N[CH2:15][CH3:16])C.[CH2:17]=O.S(=O)(=O)(O)O>>[CH2:11]([CH:10]=[C:6]([CH2:15][CH3:16])[C:7]([OH:9])=[O:8])[CH3:17].[CH2:10]([C:6](=[CH2:7])[C:1]([OH:3])=[O:2])[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 8021DiethylamineHCID 108989792-(Ethoxycarbonyl)butanoic acid

생성물 1

HCID 866430252-Ethylacrylic Acid (ethyl 2-ethylacrylate)

실험 절차

The 2-carboethoxybutyric acid obtained in step (a) was cooled to −5° C. and diethylamine was added. A solution of formalin was added dropwise into the cooled reaction mixture which was then allowed to warm to room temperature. After stirring for 24 h the reaction mixture was warmed to 60° C. and stirred for 8 h more. The mixture consisted of two layers, which were cooled to 0° C. Concentrated sulfuric acid was added and the mixture is extracted with three 200 ml portions of diethyl ether. The ether extracts were combined, dried over magnesium sulfate and filtered. The ether was removed under reduced pressure to produce ethyl 2-ethylacrylate as a yellow oil.

후처리

  1. temperaturewas warmed to 60° C.
  2. stirringstirred for 8 h more
  3. temperaturewere cooled to 0° C
  4. extractionthe mixture is extracted with three 200 ml portions of diethyl ether
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customThe ether was removed under reduced pressure

출처 및 근거

ORD 기록
ord-1f16f26fad0d4484928dff463934d3a9
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846021B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트