Sodium Hydroxide → 5-Nitro-2-thiophenecarboxaldehyde oxime

HRID 1860268

反応式

HRID 1860268 の反応式
[N+:1]([C:4]1[S:8][C:7]([CH:9]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl.[NH2:12][OH:13].[OH-].[Na+]>C(O)C.O.ClCCl>[N+:1]([C:4]1[S:8][C:7]([CH:9]=[N:12][OH:13])=[CH:6][CH:5]=1)([O-:3])=[O:2]

参加物

6

反応物 3

HCID 14798Sodium HydroxideHCID 782815-Nitrothiophene-2-carboxaldehydeHCID 443297Hydroxyamine hydrochloride

生成物 1

HCID 3505165-Nitro-2-thiophenecarboxaldehyde oxime収率 79.9%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 19096565Water ethanol溶媒

実験手順

A mixture of 5-nitrothiophene-2-carboxaldehyde (10 g, 64 mmol), hydroxylamine hydrochloride (9.4 g, 130 mmol) and sodium hydroxide (4.34 g, 107 mmol) in ethanol/water (150 ml, 2:1) was heated to reflux for 2 hours, then diluted with dichloromethane and washed with water. The organic layer was dried over magnesium sulfate and evaporated to dryness to give 8.8 g of 5-nitro-2-thiophene-carboxaldehyde oxime as a tan solid. 1H NMR (400 MHz, DMSO-d6) δ: 7.54 (1H, d), 8.13 (1H, s), 8.16 (1H, d), 13.14 (1H, s).

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 2 hours
  3. washwashed with water
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. customevaporated to dryness

出典と根拠

ORDレコード
ord-1b980d0a384e46658c2dd869af003b5c
出典データセット
uspto-grants-2003_03
特許番号
US06528653B2

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