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

Propanenitrile, 3-ethoxy- → 3-(7,8-Dimethoxy-2H-1-benzopyran-5-yl)-2-methoxymethylpropenenitrile

HRID 280028
노트
인쇄 미리보기

반응식

HRID 280028 반응식
C[O-].[Na+].[CH3:4][O:5][C:6]1[CH:15]=[C:14]([CH:16]=O)[C:9]2[CH:10]=[CH:11][CH2:12][O:13][C:8]=2[C:7]=1[O:18][CH3:19].[CH2:20]([O:22][CH2:23][CH2:24][C:25]#[N:26])C>CO.O.C(OCC)C>[CH3:4][O:5][C:6]1[CH:15]=[C:14]([CH:16]=[C:24]([CH2:23][O:22][CH3:20])[C:25]#[N:26])[C:9]2[CH:10]=[CH:11][CH2:12][O:13][C:8]=2[C:7]=1[O:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 16501Propanenitrile, 3-ethoxy-HCID 10942334Sodium MethoxideHCID 128498327,8-Dimethoxy-5-formyl-2H-1-benzopyran

생성물 1

HCID 543734473-(7,8-Dimethoxy-2H-1-benzopyran-5-yl)-2-methoxymethylpropenenitrile수율 73.6%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962
Water
용매
HCID 3283Diethyl Ether용매

실험 절차

A mixture of sodium methoxide (7.02 g, 0.13 mole), 7,8-dimethoxy-5-formyl-2H-1-benzopyran (57 g, 0.26 mole) and 3-ethoxypropanenitrile (28.35 g, 0.286 mole) in methanol (150 mL) was heated at reflux for 4 hr, allowed to cool and diluted with water (150 mL) and ethylether (500 mL). The layers were separated and the ether portion was washed with water (3×250 mL and 1×100 mL) and dried over magnesium sulfate. The ether solution was concentrated to give 55 g (73%) of an amber oil which was used without further purification.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 4 hr
  3. temperatureto cool
  4. customThe layers were separated
  5. washthe ether portion was washed with water (3×250 mL and 1×100 mL)
  6. dry with materialdried over magnesium sulfate
  7. concentrationThe ether solution was concentrated

출처 및 근거

ORD 기록
ord-1add950e2e6643c68c0380d96f543d42
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04587342

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트