Methyltriphenylphosphonium iodide → 1-Fluoro-4-methoxy-2-vinylbenzene

HRID 278050

反応式

HRID 278050 の反応式
[I-].[CH3:2][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[F:28][C:29]1[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][C:30]=1[CH:31]=O>O1CCCC1>[CH:31]([C:30]1[CH:33]=[C:34]([O:37][CH3:38])[CH:35]=[CH:36][C:29]=1[F:28])=[CH2:2]

参加物

5

反応条件

温度
0 °C

実験手順

39.4 g of methyltriphenylphosphonium iodide and 10.9 g of potassium t-butoxide were suspended in 150 ml of tetrahydrofuran. The resulting suspension was stirred at 0° C. under nitrogen stream for 30 minutes, followed by the dropwise addition thereto of a solution of 10 g of 2-fluoro-5-methoxybenzaldehyde in 20 ml of tetrahydrofuran. The resulting mixture was further stirred for one hour, quenched by the addition of water and extracted with ethyl acetate. The formed organic layer was washed with water and brine successively, dried over anhydrous magnesium sulfate, and evaporated. The resulting residue was subjected to silica gel column chromatography (developer: 5% ethyl acetate/n-hexane) to give 9.1 g of the title compound as a colorless oil.

後処理

  1. additionfollowed by the dropwise addition
  2. stirringThe resulting mixture was further stirred for one hour
  3. customquenched by the addition of water
  4. extractionextracted with ethyl acetate
  5. washThe formed organic layer was washed with water and brine successively
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customevaporated

出典と根拠

ORDレコード
ord-21d8b02e844649b2ac54108f4125b85c
出典データセット
uspto-grants-2002_03
特許番号
US06358995B1

関連ノート

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