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p-Toluenesulfonic acid → HCID 19047571, 화합물

HRID 1451336
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HRID 1451336 반응식
[O:1]1[CH:5]=[CH:4][C:3]([C:6]2(O)[C:14]3[O:13][N:12]=[C:11]([CH3:15])[C:10]=3[CH2:9][CH2:8][CH2:7]2)=[CH:2]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[O:1]1[CH:5]=[CH:4][C:3]([C:6]2[C:14]3[O:13][N:12]=[C:11]([CH3:15])[C:10]=3[CH2:9][CH2:8][CH:7]=2)=[CH:2]1
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참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 19974084HCID 19974084, 화합물

생성물 1

HCID 19047571HCID 19047571, 화합물수율 95%

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

To a mixture of 7.6 g (0.034 mol) of 7-(3-furyl)-3-methyl-4,5,6,7-tetrahydro-benzisoxazol-7-ol in 300 ml of toluene was added 100 mg of p-toluenesulfonic acid and the mixture was placed on a Rotovap, and the solvent was distilled in vacuo (80° C.) until an oil residue was obtained. Toluene (200 ml) was added to the above residue, the mixture was placed on Rotovap, and the solvent was distilled in vacuo to complete the reaction. The oil was chromatographed (silica, 1:1 hexane/methylene chloride) to afford 3.36 g (95%) of 7-(3-furyl)-3-methyl-4,5-dihydrobenzisoxazole, (Formula III: R2 =H; ##STR8## R4 =3-furanyl) as a clear oil.

후처리

  1. distillationthe solvent was distilled in vacuo (80° C.) until an oil residue
  2. customwas obtained
  3. distillationthe solvent was distilled in vacuo
  4. customthe reaction
  5. customThe oil was chromatographed (silica, 1:1 hexane/methylene chloride)

출처 및 근거

ORD 기록
ord-6c94e904714e46d2916919a67d8fc085
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05604224

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