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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Allyl bromide → HCID 10586690, 화합물

HRID 1084942
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인쇄 미리보기

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HRID 1084942 반응식
C(=O)([O-])[O-].[K+].[K+].[CH2:7](Br)[CH:8]=[CH2:9].[OH:11][C:12]1[CH:21]=[C:20]([NH:22][C:23]([CH3:25])=[O:24])[CH:19]=[CH:18][C:13]=1[C:14]([O:16][CH3:17])=[O:15]>[Cl-].C([N+](CCCC)(CCCC)CCCC)C1C=CC=CC=1.C(#N)C>[CH2:7]([O:11][C:12]1[CH:21]=[C:20]([NH:22][C:23]([CH3:25])=[O:24])[CH:19]=[CH:18][C:13]=1[C:14]([O:16][CH3:17])=[O:15])[CH:8]=[CH2:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 77719Methyl 4-acetamidosalicylate

생성물 1

HCID 10586690HCID 10586690, 화합물

시약·촉매·용매 2

HCID 159952Benzyltributylammonium chloride촉매HCID 6342Acetonitrile용매

실험 절차

138 g of potassium carbonate, 16.5 g of benzyltributylammonium chloride, 650 ml of acetonitrile and 133 g of allyl bromide were introduced into a 2-liter round-bottomed flask and 209 g of ground methyl 2-hydroxy-4-acetaminobenzoate were then added in small amounts. The contents were heated under reflux for 11 hours, a part of the acetonitrile was then distilled off and the residue was taken up with water. The precipitate formed was drained, washed with water and dried in an oven at 50° C.

후처리

  1. temperatureThe contents were heated
  2. temperatureunder reflux for 11 hours
  3. distillationa part of the acetonitrile was then distilled off
  4. customThe precipitate formed
  5. washwashed with water
  6. customdried in an oven at 50° C.

출처 및 근거

ORD 기록
ord-81098b8e6f994524a06924cf1311afc9
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05006570

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