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Dimethyl Disulfide → 3-Methyl-4-(methylthio)anisole

HRID 1892062
ノート
印刷プレビュー

反応式

HRID 1892062 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[CH3:10].C([Li])CCC.[CH3:16][S:17]SC>C1COCC1>[CH3:10][C:3]1[CH:4]=[C:5]([O:8][CH3:9])[CH:6]=[CH:7][C:2]=1[S:17][CH3:16]
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 12232Dimethyl DisulfideHCID 1179151-Bromo-4-methoxy-2-methylbenzeneHCID 178418339Butyllithium

生成物 1

HCID 5978063-Methyl-4-(methylthio)anisole収率 96.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To the cold (−78° C.) solution of 2-bromo-5-methoxy toluene (8 g, 0.04 mol) in dry THF (80 mL) under inert atmosphere, butyl lithium solution (1.6M solution in hexane; 36.8 mL, 0.058 mol) was added dropwise and the mixture was stirred for 1 h at same temperature. Dimethyl disulphide (7.7 mL, 0.08 mol) was then added dropwise and the reaction mixture was allowed to warm to room temperature over a period of 2 h. The reaction mixture was quenched with sat. ammonium chloride solution and extracted in diethyl ether. The combined organic extracts were washed with water and brine and dried. The solvent was evaporated in vacuo to yield 6.5 g of 2-methyl-4-methoxy thioanisole, which was used as such in Step 2 MS m/z 168 (M+).

後処理

  1. customThe reaction mixture was quenched with sat. ammonium chloride solution
  2. extractionextracted in diethyl ether
  3. washThe combined organic extracts were washed with water and brine
  4. customdried
  5. customThe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-fc5ab9c5daf240d9af6187c79c670ea8
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507509B2

反応ノート

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