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Morpholine → 2-(1-Naphthylmethylene)-3-(morpholinocarbonyl)propionic acid

HRID 986356
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인쇄 미리보기

반응식

HRID 986356 반응식
[C:1]1([CH:11]=[C:12]2[CH2:17][C:16](=[O:18])[O:15][C:13]2=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[NH:19]1[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1>ClCCl>[C:1]1([CH:11]=[C:12]([CH2:17][C:16]([N:19]2[CH2:24][CH2:23][O:22][CH2:21][CH2:20]2)=[O:18])[C:13]([OH:15])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8083MorpholineHCID 543164283-[(Naphthalen-1-yl)methylidene]oxolane-2,5-dione

생성물 1

HCID 545343202-(1-Naphthylmethylene)-3-(morpholinocarbonyl)propionic acid수율 80.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The solution of 1.00 g of the 2-(1-naphthylmethylene)succinic anhydride and 0.37 g of morpholine in 31 ml of dry dichloromethane was stirred for 2 hours at room temperature. The reaction mixture was evaporated under reduced pressure, and the residue was triturated with a mixture of ethyl acetate, benzene and hexane (1/1/1 by volume) to obtain 1.10 g of 2-(1-naphthylmethylene)-3-(morpholinocarbonyl)propionic acid as colorless crystals.

후처리

  1. customThe reaction mixture was evaporated under reduced pressure
  2. customthe residue was triturated with a mixture of ethyl acetate, benzene and hexane (1/1/1 by volume)

출처 및 근거

ORD 기록
ord-ccc411c7493c40708ea7fc821954fb5d
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04711958

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