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Allylamine → 2,3-Dihydro-5-(4-(1-hydroxyethyl)phenyl)-N-(2-propenyl)-2-benzofurancarboxamide

HRID 1395686
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인쇄 미리보기

반응식

HRID 1395686 반응식
[CH2:1]([NH2:4])[CH:2]=[CH2:3].[OH:5][CH:6]([C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:15]=[CH:16][C:17]3[O:21][CH:20]([C:22](OC)=[O:23])[CH2:19][C:18]=3[CH:26]=2)=[CH:10][CH:9]=1)[CH3:7]>CO>[OH:5][CH:6]([C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:15]=[CH:16][C:17]3[O:21][CH:20]([C:22]([NH:4][CH2:1][CH:2]=[CH2:3])=[O:23])[CH2:19][C:18]=3[CH:26]=2)=[CH:10][CH:9]=1)[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7853AllylamineHCID 20337915Methyl 2,3-dihydro-5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylate

생성물 1

HCID 203379102,3-Dihydro-5-(4-(1-hydroxyethyl)phenyl)-N-(2-propenyl)-2-benzofurancarboxamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

15 ml of 2-propenylamine was added to a mixture of 5.0 g of 6D and 100 ml of methanol. The solution was stirred at room temperature overnight. The volatile materials were evaporated under reduced pressure. The residue was stirred with 50 ml of ether, the solid was collected and dried in a vacuum oven to give 6, mp: 122°-124° C.

후처리

  1. customThe volatile materials were evaporated under reduced pressure
  2. stirringThe residue was stirred with 50 ml of ether
  3. customthe solid was collected
  4. customdried in a vacuum oven
  5. customto give 6, mp: 122°-124° C.

출처 및 근거

ORD 기록
ord-bd4f003d19544f8f9b9462b54020d048
출처 데이터셋
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04205080

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