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Potassium Hydroxide → 5-Cyclopentyloxy-6-methoxynicotinic acid

HRID 993286
ノート
印刷プレビュー

反応式

HRID 993286 の反応式
[OH-].[K+].[CH:3]1([O:8][C:9]2[C:10]([O:19][CH3:20])=[N:11][CH:12]=[C:13]([CH:18]=2)[C:14]([O:16]C)=[O:15])[CH2:7][CH2:6][CH2:5][CH2:4]1>O.CO>[CH:3]1([O:8][C:9]2[C:10]([O:19][CH3:20])=[N:11][CH:12]=[C:13]([CH:18]=2)[C:14]([OH:16])=[O:15])[CH2:4][CH2:5][CH2:6][CH2:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14797Potassium HydroxideHCID 22145812Methyl 5-(cyclopentyloxy)-6-methoxy-3-pyridinecarboxylate

生成物 1

HCID 221457515-Cyclopentyloxy-6-methoxynicotinic acid収率 59.3%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

A solution of potassium hydroxide (168 mg) in water (1 mL) is added to a solution of methyl 5-cyclopentyloxy-6-methoxynicotinoate (250 mg) in methanol (3 mL) and the mixture stirred for 4 hours then allowed to stand at room temperature overnight. The mixture is concentrated, the residue dissolved in water and the mixture adjusted to pH 6 by the addition of concentrated hydrochloric acid. The mixture is extracted with ethyl acetate, the extracts dried (MgSO4) and concentrated to give a cream solid. The solid is dried at 100° C. to give 5-cyclopentyloxy-6-methoxynicotinic acid (140 mg), m.p. 191-2° C. [Elemental analysis: C, 60.7; H, 6.43; N, 5.78%. calculated: C, 60.75; H, 6.37; N, 5.90%.].

後処理

  1. waitto stand at room temperature overnight
  2. concentrationThe mixture is concentrated
  3. dissolutionthe residue dissolved in water
  4. additionthe mixture adjusted to pH 6 by the addition of concentrated hydrochloric acid
  5. extractionThe mixture is extracted with ethyl acetate
  6. dry with materialthe extracts dried (MgSO4)
  7. concentrationconcentrated
  8. customto give a cream solid
  9. customThe solid is dried at 100° C.

出典と根拠

ORDレコード
ord-4997890e244f4f0cb15d547dddc655ce
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06472412B1

反応ノート

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