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Sulfuric Acid → 2-[3-(2-Methylphenyl)-5-Isoxazolyl]-Benzoic Acid

HRID 1706778
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반응식

HRID 1706778 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH2:12][C:11]2([C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[C:14](=[O:21])[O:13]2)[O:10][N:9]=1.O1CCOCC1.S(=O)(=O)(O)O>O>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:12]=[C:11]([C:20]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[C:14]([OH:21])=[O:13])[O:10][N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 312751,4-DioxaneHCID 13071254HCID 13071254, 화합물

생성물 1

HCID 131256652-[3-(2-Methylphenyl)-5-Isoxazolyl]-Benzoic Acid수율 92%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A mixture of 0.26 g. of 3'-(2-methylphenyl)-spiro[isobenzofuran-1(3H),5'(4'H)-isoxazol]-3-one, 4ml. of water, 4 ml. of dioxane and 0.10 ml. of concentrated sulfuric acid was stirred at reflux for one hour, allowed to cool and diluted with 15 ml. of water. The resultant oil was stirred several minutes to give 0.24 g. of white solid; m.p. 162°-163.5° C. in 92% yield.

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후처리

  1. additionA mixture of 0.26 g
  2. temperatureat reflux for one hour
  3. temperatureto cool
  4. additiondiluted with 15 ml
  5. customto give 0.24 g

출처 및 근거

ORD 기록
ord-49bccf5b6ccc4bc88b2673a52cdab2b2
출처 데이터셋
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04208510

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