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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethyl Disulfide → 3-Methyl-4-(methylthio)anisole

HRID 1892062
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HRID 1892062 반응식
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]
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참가 물질

5

반응물 3

HCID 12232Dimethyl DisulfideHCID 1179151-Bromo-4-methoxy-2-methylbenzeneHCID 178418339Butyllithium

생성물 1

HCID 5978063-Methyl-4-(methylthio)anisole수율 96.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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+).

후처리

  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

출처 및 근거

ORD 기록
ord-fc5ab9c5daf240d9af6187c79c670ea8
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507509B2

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