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Ethanol → HCID 23454854, 화합물

HRID 1680875
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반응식

HRID 1680875 반응식
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH:10](Cl)[C:11]([CH3:16])([N+:13]([O-:15])=[O:14])[CH3:12])=[CH:4][C:3]=2[O:2]1.Cl(O)(=O)(=O)=O.C(O)C>[H][H].C(OCC)(=O)C.[C].[Pd]>[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH2:10][C:11]([CH3:16])([N+:13]([O-:15])=[O:14])[CH3:12])=[CH:4][C:3]=2[O:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 702EthanolHCID 24247Perchloric AcidHCID 234548395-(1-Chloro-2-methyl-2-nitropropyl)-2H-1,3-benzodioxole

생성물 1

HCID 23454854HCID 23454854, 화합물수율 89%

시약·촉매·용매 3

HCID 178418390HCID 178418390, 화합물촉매HCID 8857Ethyl Acetate
용매
HCID 178418361HCID 178418361, 화합물용매

실험 절차

A mixture of 7.0 g of 1-(3,4-methylenedioxyphenyl)-1-chloro-2-methyl-2-nitropropane, 7.7 g of 70% perchloric acid, 2.8 g of 10% palladium-carbon and 100 ml of ethanol is shaken at room temperature for 3 hours in hydrogen gas atmosphere under 3 atmospheres. After the reaction, insoluble materials are removed by filtration, and the filtrate is condensed. The residue is dissolved in ethyl acetate, and the solution is washed with water, a saturated sodium bicarbonate solution and a saturated sodium chloride solution, successively. The washed solution is dried and then evaporated to remove solvent. 5.4 g of 1-(3,4-methylenedioxyphenyl)-2-methyl-2-nitropropane are thereby obtained as an oil.

후처리

  1. customAfter the reaction, insoluble materials
  2. customare removed by filtration
  3. customcondensed
  4. washthe solution is washed with water
  5. customThe washed solution is dried
  6. customevaporated
  7. customto remove solvent

출처 및 근거

ORD 기록
ord-bfac1b3d2d884b7dbc198abab3a85a5f
출처 데이터셋
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04276304

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