Methyl iodide → 1-Methylcyclohex-3-ene-1-carboxylic acid

HRID 74992

反応式

HRID 74992 の反応式
[CH:1](NC(C)C)(C)C.C([Li])CCC.[CH:13]1([C:19]([OH:21])=[O:20])[CH2:18][CH2:17][CH:16]=[CH:15][CH2:14]1.IC>C1COCC1>[CH3:1][C:13]1([C:19]([OH:21])=[O:20])[CH2:18][CH2:17][CH:16]=[CH:15][CH2:14]1

参加物

6

反応条件

温度
-78 °C

実験手順

N-isopropylpropan-2-amine (50.1 g, 69.5 mL, 495.5 mmol) was dissolved in 50 mL of THF. To the solution was added n-butyllithium (174.4 mL of 2.5 M solution in hexanes, 436.0 mmol) at −78° C. The resulting solution was stirred for 30 minutes at −78° C. To the reaction was then added cyclohex-3-ene-1-carboxylic acid (25.0 g, 198.2 mmol) and the reaction was allowed to warm to 60° C. for 2 hrs. The reaction was cooled to room temp and iodomethane (29.5 g, 13.0 mL, 208.1 mmol) was added and the reaction was allowed to stir overnight and then quenched with 1 N HCl until the pH<4. The crude product was extracted into CH2Cl2 and water. The organic phase was concentrated in vacuo to a yellow oil (27 g) and used without further purification.

後処理

  1. temperatureto warm to 60° C. for 2 hrs
  2. temperatureThe reaction was cooled to room temp
  3. stirringto stir overnight
  4. customquenched with 1 N HCl until the pH<4
  5. extractionThe crude product was extracted into CH2Cl2 and water
  6. concentrationThe organic phase was concentrated in vacuo to a yellow oil (27 g)
  7. customused without further purification

出典と根拠

ORDレコード
ord-25682a58e0934f7cb8bcc37c8d69545f
出典データセット
uspto-grants-2014_09
特許番号
US08829007B2

関連ノート

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