Methyl 6-thien-2-ylnicotinate → 6-(Thiophen-2-Yl)Pyridine-3-Carboxylic Acid

HRID 440766

反応式

HRID 440766 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:11]=[CH:10][C:9]([C:12]([O:14]C)=[O:13])=[CH:8][CH:7]=1>CO.[OH-].[Na+]>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:11]=[CH:10][C:9]([C:12]([OH:14])=[O:13])=[CH:8][CH:7]=1

参加物

4

実験手順

A solution of 2.0 g of methyl 6-(2-thienyl)pyridine-3-carboxylate in 100 ml of methyl alcohol and 50 ml of 5N sodium hydroxide is stirred at room temperature for 16 hours under nitrogen. The reaction mixture is evaporated in vacuo to about one quarter of the volume and then diluted with 150 ml of cold water. The pH is adjusted to 4 with acetic acid and the desired white product collected, washed with 400 ml of cold water until neutral. The solid is washed with 50 ml of petroleum ether and dried under vacuum to 40° C. to give the desired product.

後処理

  1. customThe reaction mixture is evaporated in vacuo to about one quarter of the volume
  2. additiondiluted with 150 ml of cold water
  3. customthe desired white product collected
  4. washwashed with 400 ml of cold water until neutral
  5. washThe solid is washed with 50 ml of petroleum ether
  6. customdried under vacuum to 40° C.

出典と根拠

ORDレコード
ord-99a7d22472914ee8a67a8d1bd0cba47d
出典データセット
uspto-grants-1996_05
特許番号
US05521173

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