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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → 647833-71-4

HRID 1445324
ノート
印刷プレビュー

反応式

HRID 1445324 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([C:11]2[S:12][CH:13]=[CH:14][C:15]=2[O:16]C)=[O:10])=[CH:5][CH:4]=1.O>ClCCl>[OH:16][C:15]1[CH:14]=[CH:13][S:12][C:11]=1[C:9]([C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 962WaterHCID 21961240(4-Methoxyphenyl)(3-methoxythiophen-2-yl)methanone

生成物 1

HCID 135744175647833-71-4

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

993 mg of (4-methoxy-phenyl)-(3-methoxy-thiophen-2-yl)-methanone were dissolved in 20 ml of dry dichloromethane, and 7 ml of boron tribromide/dimethyl sulfide complex were added. The mixture was stirred at room temp. until the reaction was complete (TLC check). It was then poured into water and extracted several times with dichloromethane. The organic phase was dried and concentrated, and the residue was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:4). The product with the molecular weight of 234.3 (C12H10O3S), MS (Cl): 235 (M+H+) was obtained.

後処理

  1. addition7 ml of boron tribromide/dimethyl sulfide complex were added
  2. extractionextracted several times with dichloromethane
  3. customThe organic phase was dried
  4. concentrationconcentrated
  5. customthe residue was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:4)
  6. customThe product with the molecular weight of 234.3 (C12H10O3S), MS (Cl): 235 (M+H+) was obtained

出典と根拠

ORDレコード
ord-7b3c4556084e44a38e2e03868d36fbd6
出典データセット
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07666848B2

反応ノート

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