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2-(6-Methoxy-2-naphthyl)propionic acid → 2-(6-Methoxynaphthalen-2-yl)propanoic acid--ethanamine (1/1)

HRID 1607488
노트
인쇄 미리보기

반응식

HRID 1607488 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([CH3:17])[C:14]([OH:16])=[O:15])[CH:7]=[CH:6]2.[CH2:18]([NH2:20])[CH3:19]>CC(C)=O>[CH2:18]([NH2:20])[CH3:19].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([CH3:17])[C:14]([OH:16])=[O:15])[CH:7]=[CH:6]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 13022-(6-Methoxy-2-naphthyl)propionic acidHCID 6341Ethylamine

생성물 1

HCID 441538962-(6-Methoxynaphthalen-2-yl)propanoic acid--ethanamine (1/1)

시약·촉매·용매 1

HCID 180Acetone용매

반응 조건

온도
25 °C

실험 절차

230 g (1 mole) of (±)-2-(6-methoxy-2-naphthyl) propionic acid was dissolved in 1.5 l of acetone at about 45° C. By addition of 64 g (1 mole) of a 70% w/w aqueous monoethylamine solution, the ethylamine salt crystallized. The mixture was cooled to about 25° C., filtered and washed portionwise with 200 ml of acetone.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customthe ethylamine salt crystallized
  2. filtrationfiltered
  3. washwashed portionwise with 200 ml of acetone

출처 및 근거

ORD 기록
ord-2285ac221bcd47ad96639dd2f910b1c6
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04865770

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