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Hydrochloric Acid → N,3-Dihydroxypyridine-4-carboxamide

HRID 2222585
ノート
印刷プレビュー

反応式

HRID 2222585 の反応式
[OH:1][C:2]1[CH:11]=[N:10][CH:9]=[CH:8][C:3]=1[C:4](OC)=[O:5].Cl.[NH2:13][OH:14].[OH-].[Na+].Cl>>[OH:1][C:2]1[CH:11]=[N:10][CH:9]=[CH:8][C:3]=1[C:4]([NH:13][OH:14])=[O:5]
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 4

HCID 313Hydrochloric Acid2 回HCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 12414071Methyl 3-hydroxypyridine-4-carboxylate

生成物 1

HCID 45123502N,3-Dihydroxypyridine-4-carboxamide収率 96%

実験手順

To a stirred suspension of methyl 3-hydroxy-isonicotinate (176 g; 1.15 mol) in water/ice (50/50, 1700 mL), was added hydroxylamine hydrochloride (127.9 g; 1.84 mol). The temperature fell to −5° C. and then aqueous NaOH solution (454 mL, 28% w/v) was added dropwise keeping the temperature below 5° C. during the addition. Hereafter the reaction mixture was stirred at ambient temperature for 1.5 h followed by heating to 60° C. At this temperature the pH was adjusted to 5.4 by the addition of aqueous hydrochloric acid (10 M) at which point a heavy precipitate forms. The reaction mixture was then stirred at ambient temperature followed by cooling to 5° C. The pH was then adjusted to 4.0 by the addition of aqueous hydrochloric acid (10 M), and then was stirred whilst cold for 1.5 h. The crystals were filtered off, rinsed with water (3×100 mL), dried on the filter and then dried further at reduced pressure and 40° C. overnight to give 3,N-dihydroxy-isonicotinamide (169.3 g, 96%; HPLC purity 98%) as a white solid.

後処理

  1. customfell to −5° C.
  2. customthe temperature below 5° C.
  3. additionduring the addition
  4. temperatureby heating to 60° C
  5. stirringThe reaction mixture was then stirred at ambient temperature
  6. temperatureby cooling to 5° C
  7. stirringwas stirred whilst cold for 1.5 h
  8. filtrationThe crystals were filtered off
  9. washrinsed with water (3×100 mL)
  10. customdried on the
  11. filtrationfilter
  12. customdried further at reduced pressure and 40° C. overnight

出典と根拠

ORDレコード
ord-0f18a5f623304a5c82ad161bb29e7190
出典データセット
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07371863B2

反応ノート

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