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Methanol → Methyl 2-(3-methylisoxazol-5-yl)acetate

HRID 922242
ノート
印刷プレビュー

反応式

HRID 922242 の反応式
[CH3:1][C:2]1[CH:6]=[C:5]([CH2:7][C:8]([OH:10])=[O:9])[O:4][N:3]=1.O=S(Cl)Cl.[CH3:15]O>>[CH3:1][C:2]1[CH:6]=[C:5]([CH2:7][C:8]([O:10][CH3:15])=[O:9])[O:4][N:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 41955322-(3-Methyl-1,2-oxazol-5-yl)acetic acid

生成物 1

HCID 12366875Methyl 2-(3-methylisoxazol-5-yl)acetate収率 92%

反応条件

温度
50 °C

実験手順

To a 50 mL RB flask fitted with magnetic stirrer was charged with 10 mL of methanol. To the stirred solvent was added (3-methyl-1,2-oxazol-5-yl)acetic acid (1 g, 7 mmol), was added drop wise SOCl2 (1.25 g, 10.5 mmol) to the reaction mixture at 0° C. and stirred at 50° C. for 4 h. After completion of the reaction, the reaction mixture was concentrated to distill off the solvent; water (25 mL) was added and extracted with ethyl acetate (25 mL). The organic layer was washed with saturated NaHCO3 solution (10 mL) and brine solution (10 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product was obtained as brown liquid (1 g, yield: 92%). 1H NMR (300 MHz, CDCl3): δ 6.03 (s, 1H), 3.73 (d, 2H), 3.69 (s, 3H), 2.23 (s, 3H).

後処理

  1. customTo a 50 mL RB flask fitted with magnetic stirrer
  2. customAfter completion of the reaction
  3. concentrationthe reaction mixture was concentrated
  4. distillationto distill off the solvent
  5. additionwater (25 mL) was added
  6. extractionextracted with ethyl acetate (25 mL)
  7. washThe organic layer was washed with saturated NaHCO3 solution (10 mL) and brine solution (10 mL)
  8. dry with materialThe organic layer was dried over anhydrous Na2SO4
  9. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-72bdaca1cb1d4376b22829b5a30417bf
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09278915B2

反応ノート

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