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Ethanolamine → HCID 12906351, 화합물

HRID 461222
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HRID 461222 반응식
[C:1]([CH:3]1[CH:12]2[C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:18]=3[CH:5]([C:6]3[C:11]2=[CH:10][CH:9]=[CH:8][CH:7]=3)[CH2:4]1)#[N:2].[CH2:19]([CH2:21]N)[OH:20]>C1C=CC=CC=1.C([O-])(=O)C.[Zn+2].C([O-])(=O)C>[O:20]1[CH2:19][CH2:21][N:2]=[C:1]1[CH:3]1[CH:12]2[C:11]3[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=3[CH:5]([C:18]3[C:13]2=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:4]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 700EthanolamineHCID 2403069,10-Dihydro-9,10-ethanoanthracene-11-carbonitrile

생성물 1

HCID 12906351HCID 12906351, 화합물수율 60.3%

시약·촉매·용매 2

HCID 11192Zinc Acetate촉매HCID 241Benzene용매

반응 조건

온도
130 °C

실험 절차

A mixture of 11-cyano-9,10-dihydro-9,10-ethanoanthracene (4.6 g), ethanolamine (1.8 g) and zinc acetate (250 mg) is stirred at 130° C for 5 hours. The reaction mixture is dissolved in benzene and passed through a column of 10% hydrated alumina. The eluate is evaporated to remove the solvent, and the residue is recrystallized from ether to give 11-(2-oxazolin-2-yl)-9,10-dihydro-9,10-ethanoanthracene (3.3 g) as crystals melting at 155° to 156° C. IR (KRr), 1655 cm-1 (O--C=N).

후처리

  1. customThe eluate is evaporated
  2. customto remove the solvent
  3. customthe residue is recrystallized from ether

출처 및 근거

ORD 기록
ord-d214ae2f8e5542109790b4c42a8477cc
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04061854

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