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Piperonal → 5-Benzo[1,3]dioxol-5-yl-oxazole

HRID 917661
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HRID 917661 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]=[O:11])=[CH:9][C:4]=2[O:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+].[N+:18]([CH2:20]S(C1C=CC(C)=CC=1)(=O)=O)#[C-:19]>CO>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]3[O:11][CH:20]=[N:18][CH:19]=3)=[CH:9][C:4]=2[O:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 8438PiperonalHCID 11430Potassium CarbonateHCID 161915Tosylmethyl isocyanide

생성물 1

HCID 106791935-Benzo[1,3]dioxol-5-yl-oxazole수율 82%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
70 °C

실험 절차

To a stirred solution of benzo[1,3]dioxole-5-carbaldehyde (657 mg, 4.83 mmol) in methanol (15 mL) was added potassium carbonate (786 mg, 5.69 mmol, 1.3 equiv) and 1-isocyanomethanesulfonyl-4-methyl-benzene (863 mg, 4.38 mmol, 1 equiv). The resulting solution was heated to 70° C. under a nitrogen atmosphere for 3 hours, cooled to ambient temperature, and concentrated in vacuo. The residue was partitioned between methylene chloride and water, and the aqueous layer was extracted three times with methylene chloride. The combined organic layers were dried over sodium sulfate and concentrated in vacuo. Silica gel chromatography (30% ethyl acetate in hexanes) provided 5-benzo[1,3]dioxol-5-yl-oxazole (676 mg, 82%).

후처리

  1. temperaturecooled to ambient temperature
  2. concentrationconcentrated in vacuo
  3. customThe residue was partitioned between methylene chloride and water
  4. extractionthe aqueous layer was extracted three times with methylene chloride
  5. dry with materialThe combined organic layers were dried over sodium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9185134dfacf4d4c87fec07913a1e7c0
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07273936B2

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