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

Lithium Hydroxide → (Z)-3-(2-naphthyl)prop-2-enoic acid

HRID 1934885
노트
인쇄 미리보기

반응식

HRID 1934885 반응식
C([O:3][C:4](=[O:17])/[CH:5]=[CH:6]\[C:7]1[CH:16]=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=1)C.[OH-].[Li+]>O1CCCC1.O>[CH:8]1[C:9]2[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:15]=[CH:16][C:7]=1/[CH:6]=[CH:5]\[C:4]([OH:17])=[O:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 3939Lithium HydroxideHCID 69822035HCID 69822035, 화합물

생성물 1

HCID 1712266(Z)-3-(2-naphthyl)prop-2-enoic acid

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

A solution of (Z)-naphthalene-2-acrylic acid ethyl ester (1.38 g, 6.0 mmole) in a mixture of tetrahydrofuran (10 ml) and water (10 ml) was treated with lithium hydroxide (0.88 g, 37 mmol) and heated to 60° C. for 6 hours. On cooling, the organic phase was separated and the. aqueous phase was acidified and extracted with diethyl ether. The ethereal phase was dried and the solvent removed in vaccuo to give (Z)-3-(2-naphthyl)prop-2-enoic acid as a white solid which was used without further purification, Mp 207-209° C.

후처리

  1. temperatureOn cooling
  2. customthe organic phase was separated
  3. extractionextracted with diethyl ether
  4. customThe ethereal phase was dried
  5. customthe solvent removed in vaccuo

출처 및 근거

ORD 기록
ord-5c83ca8faea3465d9942c2adaa21da38
출처 데이터셋
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06384281B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트