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Water → N-(3-Carbomethoxy-5-methyl-2-thienyl)-2-methylpropanamide

HRID 1448708
ノート
印刷プレビュー

反応式

HRID 1448708 の反応式
[C:1](Cl)(=[O:5])[CH:2]([CH3:4])[CH3:3].[CH3:7][O:8][C:9]([C:11]1[CH:15]=[C:14]([CH3:16])[S:13][C:12]=1[NH2:17])=[O:10].O>CN(C)P(N(C)C)(N(C)C)=O>[C:9]([C:11]1[CH:15]=[C:14]([CH3:16])[S:13][C:12]=1[NH:17][C:1](=[O:5])[CH:2]([CH3:4])[CH3:3])([O:8][CH3:7])=[O:10]
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 3

HCID 962WaterHCID 62325Isobutyryl chlorideHCID 675878Methyl-2-amino-5-methyl-3-thiophenecarboxylate

生成物 1

HCID 23341602N-(3-Carbomethoxy-5-methyl-2-thienyl)-2-methylpropanamide収率 88%

試薬・触媒・溶媒 1

HCID 12679Hexamethylphosphoramide溶媒

実験手順

isoButyryl chloride (22.4 g) was added dropwise during 40 minutes to a stirred solution of methyl-2-amino-5-methyl-3-thiophenecarboxylate (34.2 g, 0.2 mol) in dry hexamethylphosphoramide (100 ml) kept at 5°-10° C. This temperature was maintained for a further 1 hour and then the reaction was kept at room temperature for 16 hours. The reaction mixture was poured into water (1600 ml) and the yellow precipitate was filtered off, washed with water and dried at 50° C. Recrystallisation of the solid from petroleum ether (b.p. 60°-80° C. yielded cream crystals (39.6 g, 88%), m.p. 63°-65° C.

後処理

  1. customkept at 5°-10° C
  2. temperatureThis temperature was maintained for a further 1 hour
  3. filtrationthe yellow precipitate was filtered off
  4. washwashed with water
  5. customdried at 50° C
  6. customRecrystallisation of the solid from petroleum ether (b.p. 60°-80° C.

出典と根拠

ORDレコード
ord-3cbebfc80e164b7d9949587bd96d1718
出典データセット
uspto-grants-1980_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04187232

反応ノート

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