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Water → HCID 11608549, 화합물

HRID 1831614
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HRID 1831614 반응식
[NH2:1][C:2]1[CH:9]=[C:8]2[O:10][CH2:11][O:12][C:7]2=[CH:6][C:3]=1[C:4]#N.[CH2:13]([Mg]Cl)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.O.[OH:23]S(O)(=O)=O>C1COCC1.CCOCC>[NH2:1][C:2]1[CH:9]=[C:8]2[O:10][CH2:11][O:12][C:7]2=[CH:6][C:3]=1[C:4]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 1118Sulfuric AcidHCID 6879796-Amino-1,3-benzodioxole-5-carbonitrileHCID 178418336HCID 178418336, 화합물

생성물 1

HCID 11608549HCID 11608549, 화합물수율 52%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8028
Tetrahydrofuran
용매

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온도
25 °C

실험 절차

To a stirred solution of 1.5 g (10.0 mmol) of 2-amino-4,5-methylenedioxy-benzonitrile in THF (40 mL) was added CuBr (50 mg, 0.34 mmol) and benzylmagnesium chloride (40 mL, 1.0 M solution in Et2O). The reaction mixture was refluxed for 12 h. After cooling to 25° C., H2O (5 mL) was added followed by 15% H2SO4 (15 mL). After stirring for 14 h, ether (50 mL) was added. Organic layer was separated. Aqueous layer was extracted with ether (2×50 mL). The combined organic layer was dried and evaporated. Following chromatography (silica gel, CHCl3), 1.2 g (52%) of the title compound was obtained. IR (CHCl3) 1675 cm−1 MS m/z 255 (M+).

후처리

  1. temperatureThe reaction mixture was refluxed for 12 h
  2. customOrganic layer was separated
  3. extractionAqueous layer was extracted with ether (2×50 mL)
  4. customThe combined organic layer was dried
  5. customevaporated

출처 및 근거

ORD 기록
ord-9aab117bfd1c4b4ca14b13dc01775781
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067666B2

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