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Dimethyl Sulfide → 1-[(E)-3-Chloro-1-methyl-1-propenyl]-3-nitrobenzene

HRID 1826401
ノート
印刷プレビュー

反応式

HRID 1826401 の反応式
[Cl:1]N1C(=O)CCC1=O.CSC.[N+:12]([C:15]1[CH:16]=[C:17](/[C:21](/[CH3:25])=[CH:22]/[CH2:23]O)[CH:18]=[CH:19][CH:20]=1)([O-:14])=[O:13]>ClCCl>[Cl:1][CH2:23]/[CH:22]=[C:21](/[C:17]1[CH:18]=[CH:19][CH:20]=[C:15]([N+:12]([O-:14])=[O:13])[CH:16]=1)\[CH3:25]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1068Dimethyl SulfideHCID 31398ChlorosuccinimideHCID 69554909(E)-3-(3-nitrophenyl)-2-buten-1-ol

生成物 1

HCID 695554961-[(E)-3-Chloro-1-methyl-1-propenyl]-3-nitrobenzene

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of N-chlorosuccinimide (52.3 g, 0.39 mol) in dichloromethane (800 ml) at 0° C. was added dropwise over 1 h dimethylsulfide (27.9 ml, 0.38 mol). To the mixture was added dropwise over 30 min at 0° C. a solution of (E)-3-(3-nitrophenyl)-2-buten-1-ol (Preparation 2, 72 g, 0.373 mol) in dichloromethane (200 ml). The mixture was warmed to room temperature over 1 h, then poured onto brine (500 ml). The layers were separated, and the aqueous layer extracted with ether (500 ml). The organic extracts were combined, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica column chromatography, eluting with 10:1 hexane/ethyl acetate, then as a gradient up to 4:1 hexane/ethyl acetate. Appropriate fractions were combined and concentrated in vacuo to give the title compound as a very pale yellow solid (69 g, 88%).

後処理

  1. additionpoured onto brine (500 ml)
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted with ether (500 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by silica column chromatography
  8. washeluting with 10:1 hexane/ethyl acetate
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-bfe0784f90034766b736d39f4b61c8e3
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07049444B2

反応ノート

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