Methyl iodide → HCID 15733061、化合物

HRID 486040ノート

反応式

HRID 486040 の反応式
[CH3:1]I.[Mg].[Cl-].[C:5]1([CH2:11][N+:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([CH3:19])[CH:13]=2)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[Cl-].[NH4+]>CCOCC>[C:5]1([CH2:11][N:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([CH3:19])[CH:13]2[CH3:1])[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1

参加物

6

実験手順

A solution of methyl iodide (112 mL, 1.8 mole) in ether (225 mL) was added dropwise to a suspension of magnesium turnings (44 g, 1.8 mole) in ether (225 ml) under nitrogen over a period of 1 hour. The mixture was stirred at room temperature for 1 hour, transferred into a 1000 mL addition funnel and then was added to a suspension of N-(phenylmethyl)-3,4-dimethylpyridinium chloride (350.7 g, 1.5 mole) in ether (1500 mL) under a nitrogen atmosphere. The reaction mixture was stirred at room temperature for 24 hours and was then poured into a solution of saturated ammonium chloride (3 L). The organic layer was separated and the aqueous layer was extracted with ether (1000 mL). The combined ether layers were washed with water (500 mL), then brine (500 mL) and were dried over sodium sulfate and potassium carbonate-. The solvent was removed in vacuo to afford 284.1 g (76%) of 1,2-dihydro-N-(phenylmethyl)-2,3,4-trimethylpyridine, as an amber oil.

後処理

  1. additiontransferred into a 1000 mL addition funnel
  2. stirringThe reaction mixture was stirred at room temperature for 24 hours
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with ether (1000 mL)
  5. washThe combined ether layers were washed with water (500 mL)
  6. dry with materialbrine (500 mL) and were dried over sodium sulfate and potassium carbonate-
  7. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-1bb1ec699b104dd385f0c82db94863af
出典データセット
uspto-grants-1994_03
特許番号
US05290789

反応ノート

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