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

Diethyl Carbonate → Ethyl cyano(3,4-dimethoxyphenyl)acetate

HRID 1464149
노트
인쇄 미리보기

반응식

HRID 1464149 반응식
[Na].[C:2](#[N:14])[CH2:3][C:4]1[CH:13]=[CH:12][C:9]([O:10][CH3:11])=[C:6]([O:7][CH3:8])[CH:5]=1.[C:15](=O)([O:19]CC)[O:16][CH2:17][CH3:18]>>[CH3:8][O:7][C:6]1[CH:5]=[C:4]([CH:3]([C:2]#[N:14])[C:15]([O:16][CH2:17][CH3:18])=[O:19])[CH:13]=[CH:12][C:9]=1[O:10][CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7766Diethyl CarbonateHCID 667273,4-DimethoxybenzeneacetonitrileHCID 5360545Sodium

생성물 1

HCID 12814070Ethyl cyano(3,4-dimethoxyphenyl)acetate

실험 절차

25.7 g (1.1 mol eq.) of sodium in small pieces were added gradually to a solution of 198 g (1.1 mol) of homoveratronitrile in 500 ml of diethyl carbonate in such a manner that the temperature remained at approximately 100°. Thereafter, the reaction mixture was heated to reflux for 1 hour, evaporated under reduced pressure, treated with cooled water, acidified with 70 ml of glacial acetic acid and extracted with ether. The combined organic extracts were dried and evaporated. The residual oil was distilled in a high vacuum, whereby ethyl 3,4-dimethoxyphenylcyanoacetate was obtained, b.p. 170°-172°/70 Pa. HPLC purity >99%.

후처리

  1. customremained at approximately 100°
  2. temperatureThereafter, the reaction mixture was heated
  3. temperatureto reflux for 1 hour
  4. customevaporated under reduced pressure
  5. additiontreated with cooled water
  6. extractionextracted with ether
  7. customThe combined organic extracts were dried
  8. customevaporated
  9. distillationThe residual oil was distilled in a high vacuum

출처 및 근거

ORD 기록
ord-8c7fb1d8e9df4f73a3106f56b95f2adc
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05302727

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트