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

Ethyl Acetate → 3-[3-(3-Thienyl)phenoxy] propanal dimethylacetal

HRID 1464769
노트
인쇄 미리보기

반응식

HRID 1464769 반응식
[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:7]=[C:8]([OH:12])[CH:9]=[CH:10][CH:11]=2)=[CH:2]1.[CH3:13][O:14][CH:15]([O:19][CH3:20])[CH2:16][CH2:17]Br.C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C>CN(C)C=O.O>[CH3:13][O:14][CH:15]([O:19][CH3:20])[CH2:16][CH2:17][O:12][C:8]1[CH:9]=[CH:10][CH:11]=[C:6]([C:3]2[CH:4]=[CH:5][S:1][CH:2]=2)[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 1189323-Bromopropionaldehyde dimethylacetalHCID 41303433-(Thiophen-3-YL)phenol

생성물 1

HCID 199170573-[3-(3-Thienyl)phenoxy] propanal dimethylacetal

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

반응 조건

온도
90 °C

실험 절차

1.3 g of 3-(3-thienyl)phenol, 1.09 ml of 3-bromopropanal dimethylacetal and 1.1 g of potassium carbonate were dissolved in 10 ml of dimethylformamide, and the mixture was heated at 90° C. with stirring for 6 hours. Ethyl acetate and water were added, and the organic layer separated was worked up in a customary manner, then the product was purified by silica gel column chromatography [hexane / ethyl acetate=30/1→20/1] to give 1.0 g of 3-[3-(3-thienyl)phenoxy] propanal dimethylacetal as a colorless oil.

후처리

  1. customthe organic layer separated
  2. customthe product was purified by silica gel column chromatography [hexane / ethyl acetate=30/1→20/1]

출처 및 근거

ORD 기록
ord-4c11c325e40045ff9cb39e902e35bc2d
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05306728

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트