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Hexamethylenetetramine → Ethyl 2-(4-formylphenyl)acetate

HRID 377608
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인쇄 미리보기

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HRID 377608 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:5][CH:4]=1.C1N2CN3CN(C2)CN1C3.C(=O)([O-])[O-:26].[Na+].[Na+]>C(O)(=O)C>[CH:2]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:5][CH:4]=1)=[O:26]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 4101HexamethylenetetramineHCID 10340Sodium CarbonateHCID 15712209Ethyl 2-(4-(bromomethyl)phenyl)acetate

생성물 1

HCID 11310039Ethyl 2-(4-formylphenyl)acetate

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
100 °C

실험 절차

25.7 g of ethyl 4-bromomethylphenylacetate and 28 g of hexamethylenetetramine are dissolved in 200 ml of 20% acetic acid, heated to 100° C. with stirring and stirred for four hours. The reaction solution is allowed to cool and sufficient sodium carbonate is added until a saturated solution is obtained. This solution is extracted with ether, dried and the ether is then removed. The residue is purified by chromatography (silica gel/methyl t-butyl ether/ether 1:1).

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후처리

  1. stirringstirred for four hours
  2. temperatureto cool
  3. customis obtained
  4. extractionThis solution is extracted with ether
  5. customdried
  6. customthe ether is then removed
  7. customThe residue is purified by chromatography (silica gel/methyl t-butyl ether/ether 1:1)

출처 및 근거

ORD 기록
ord-f366f9710245485a8febd1a7159c7a7d
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06028080

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