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Dichloroacetyl chloride → HCID 4158166、化合物

HRID 2398095
ノート
印刷プレビュー

反応式

HRID 2398095 の反応式
[N+:1]([C:4]1[O:8][C:7]([CH:9]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[Cl:11][CH:12]([Cl:16])C(Cl)=O.C(N(CC)CC)C>C1C=CC=CC=1>[Cl:11][C:12]([Cl:16])=[CH:9][C:7]1[O:8][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=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 3

HCID 6593Dichloroacetyl chlorideHCID 8471TriethylamineHCID 127745-Nitrofurfural

生成物 1

HCID 4158166HCID 4158166、化合物

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

To a stirred mixture of 14.1 g of 5-nitro-2-furaldehyde and 22.1 g of dichloroacetyl chloride in 300 ml of benzene was added dropwise at 25°-30° over a 30-minute period a solution of 15.2 g of triethylamine in 50 ml of benzene. The mixture then was stirred at 25°-30° for an additional 30 minutes and then for 90 minutes at reflux. After cooling, the mixture was filtered and the filtrate was washed and dried, concentrated under reduced pressure and Claisen distilled to give a liquid product, b.p.: 88°-98° at 0.3 torr. (mainly 90°-95°). This material was crystallized from acetone/petroleum ether to give 1 as a light yellow solid, m.p.: 74°-75°.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturefor 90 minutes at reflux
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. washthe filtrate was washed
  5. customdried
  6. concentrationconcentrated under reduced pressure and Claisen
  7. distillationdistilled
  8. customto give a liquid product, b.p.: 88°-98° at 0.3 torr
  9. custommainly 90°-95°
  10. customThis material was crystallized from acetone/petroleum ether

出典と根拠

ORDレコード
ord-daaaeac386c348b5bb5b6df8d0063b5f
出典データセット
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04024161

反応ノート

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