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Water → p-Trimethylgermylacetophenone

HRID 613162
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반응식

HRID 613162 반응식
[CH3:1][Ge:2]([CH3:16])([CH3:15])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2([CH3:14])OCC[O:10]2)=[CH:5][CH:4]=1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.O>CC(C)=O>[CH3:15][Ge:2]([CH3:1])([CH3:16])[C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:10])[CH3:14])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 146056512-(4-Trimethylgermylphenyl)-2-methyl-1,3-dioxolane

생성물 1

HCID 14605652p-Trimethylgermylacetophenone

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A solution of 420 mg (1.5 mmol) of 2-(4-trimethylgermylphenyl)-2-methyl-1,3-dioxolane and 56 mg (0.19 mmol) of pyridinium p-toluenesulfonate (PPTS) in 1.35 g (62.5 mmol) of water and 10 ml of acetone was refluxed for 2 hours and stirred at room temperature for 1.5 days. The reaction mixture was extracted with petroleum ether. The extract was washed successively with 2N hydrochloric acid, water and sat.aq.NaHCO3, dried and evaporated.

후처리

  1. extractionThe reaction mixture was extracted with petroleum ether
  2. washThe extract was washed successively with 2N hydrochloric acid, water and sat.aq
  3. dry with materialNaHCO3, dried
  4. customevaporated

출처 및 근거

ORD 기록
ord-cdc04f6b79a14fe5b056d91cbc196702
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE036477

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