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Potassium Carbonate → 2-n-Butyl-3-[4-(2,3-epoxypropoxy)phenylsulfonyl]benzofuran

HRID 1764663
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HRID 1764663 반응식
[CH2:1]([C:5]1[O:6][C:7]2[CH:23]=[CH:22][CH:21]=[CH:20][C:8]=2[C:9]=1[S:10]([C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=1)(=[O:12])=[O:11])[CH2:2][CH2:3][CH3:4].C(=O)([O-])[O-].[K+].[K+].[CH2:30]([CH:32]1[O:34][CH2:33]1)Br>CC(C)=O>[CH2:1]([C:5]1[O:6][C:7]2[CH:23]=[CH:22][CH:21]=[CH:20][C:8]=2[C:9]=1[S:10]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:30][CH:32]2[O:34][CH2:33]2)=[CH:15][CH:14]=1)(=[O:12])=[O:11])[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 18430EpibromohydrinHCID 149563642-n-Butyl-3-(4-hydroxyphenylsulfonyl)benzofuran

생성물 1

HCID 227688372-n-Butyl-3-[4-(2,3-epoxypropoxy)phenylsulfonyl]benzofuran

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

2-n-Butyl-3-(4-hydroxyphenylsulfonyl)benzofuran (1.5 g., 0.0045 mol.) was dissolved in 40 ml. of dry acetone containing 2.5 g. (0.018 mol.) of potassium carbonate and 2.46 g. (0.018 mol.) of epibromohydrin. The mixture was refluxed for ca. 16 hours then filtered. The solvent and excess epibromohydrin were removed in vacuo to give 2-n-butyl-3-[4-(2,3-epoxypropoxy)phenylsulfonyl]benzofuran.

후처리

  1. temperatureThe mixture was refluxed for ca. 16 hours
  2. filtrationthen filtered
  3. customThe solvent and excess epibromohydrin were removed in vacuo

출처 및 근거

ORD 기록
ord-5b7709ca6bb14565b04340e0e9d48895
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04117128

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