Potassium Hydroxide → 3-(Methylsulfanyl)pentanoic acid

HRID 1484756

反応式

HRID 1484756 の反応式
[C:1](SC)(=O)[S:2]C.[C:7]([OH:13])(=[O:12])/[CH:8]=[CH:9]/[CH2:10][CH3:11].[OH-].[K+]>>[CH3:1][S:2][CH:9]([CH2:10][CH3:11])[CH2:8][C:7]([OH:13])=[O:12]

参加物

4

反応条件

温度
90 °C

実験手順

S,S-dimethyl carbonodithioate (1.467 g, 12.00 mmol) was added with vigorous stirring to a solution of (E)-pent-2-enoic acid (2.002 g, 20 mmol) in 30% KOH solution (prepared from potassium hydroxide (3.87 g, 69 mmol) and Water (10 mL)). The reaction mixture was slowly heated to 90° C. over a period of 20-30 min. Heating was continued for 3 hours before the reaction was cooled down to 25° C. and quenched slowly with HCl. The mixture was then extracted with DCM (3×30 mL), combined organic layer dried and concentrated to give 3-(methylthio)pentanoic acid (2.7 g, 18.22 mmol, 91% yield) as light orange oil: IR (Thin film) 2975, 1701 cm−1; 1H NMR (400 MHz, CDCl3) δ 2.92 (qd, J=7.3, 5.6 Hz, 1H), 2.63 (d, J=7.2 Hz, 2H), 2.08 (s, 3H), 1.75-1.51 (m, 2H), 1.03 (t, J=7.4 Hz, 3H); 13C NMR (101 MHz, CDCl3) δ 178.14, 43.95, 39.78, 27.04, 12.95, 11.29; EIMS m/z 148.

後処理

  1. temperatureHeating
  2. temperaturewas cooled down to 25° C.
  3. customquenched slowly with HCl
  4. extractionThe mixture was then extracted with DCM (3×30 mL)
  5. customdried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-ef8fee6d063e48849010a96cf8828089
出典データセット
uspto-grants-2016_08
特許番号
US09422278B2

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