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

Methanol → methyl (E)-beta-methoxy-2-methylcinnamate

HRID 1899781
노트
인쇄 미리보기

반응식

HRID 1899781 반응식
[CH:1]([O:6]C)([O:4][CH3:5])OC.[CH3:8][OH:9].OS(O)(=O)=O.N1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[CH3:8][O:9]/[C:17](/[C:18]1[CH:19]=[CH:18][CH:17]=[CH:16][C:19]=1[CH3:20])=[CH:16]/[C:1]([O:4][CH3:5])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 887MethanolHCID 1049PyridineHCID 1118Sulfuric AcidHCID 9005Trimethyl orthoformate

생성물 1

HCID 86749647methyl (E)-beta-methoxy-2-methylcinnamate수율 94%

실험 절차

A mixture of 1280 g (6.7 mol ) of methyl 2-methylbenzoyl acetate, 848 g (8.0 mol) of trimethyl orthoformate, 400 ml of methanol and 10 ml of concentrated H2SO4 is stirred at room temperature for 12 h. The mixture is subsequently neutralized with 20 ml of pyridine and then concentrated, and the residue is fractionally distilled (boiling point 120-123° C./0.6 torr). 1300 g (94%) of methyl (E)-β-methoxy-2-methylcinnamate are obtained as a pale yellow oil.

후처리

  1. concentrationconcentrated
  2. distillationthe residue is fractionally distilled (boiling point 120-123° C./0.6 torr)

출처 및 근거

ORD 기록
ord-5e3e51b0e28a4f98b1ee175aa8007313
출처 데이터셋
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05573999

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트