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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Aniline → Chloroacetanilide

HRID 38707
ノート
印刷プレビュー

反応式

HRID 38707 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[Cl:15][CH2:16][C:17](Cl)=[O:18]>C1COCC1>[Cl:15][CH2:16][C:17]([NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:18]
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 6115AnilineHCID 6577Chloroacetyl chlorideHCID 8471Triethylamine

生成物 1

HCID 11485Chloroacetanilide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of aniline (9.31 g, 100 mmol) and triethylamine (15.2 g, 150 mmol) in THF (150 mL) is cooled to −40° C. before chloroacetic acid chloride (11.3 g, 100 mmol) is slowly added in portions such that the temperature does not rise above 0° C. After completion of the addition, the brown suspension is stirred at rt for 1 h. The dark purple mixture is poured onto water (300 mL) and extracted twice with EA (300 mL). The organic extracts are washed with sat. aq. NaHCO3, 0.5 N aq. HCl, followed by water, and evaporated. The brown residue is suspended in diethyl ether, filtered off, washed with additional diethyl ether and dried under high vacuum to give 2-chloro-N-phenyl-acetamide. LC-MS: tR=0.75 min, [M+1]+=170, 1H NMR (CDCl3): δ 8.22 (s br, 1H), 7.56-7.51 (m, 2H), 7.40-7.24 (m, 2H), 7.20-7.14 (m, 1H), 4.20 (s, 2H).

後処理

  1. additionis slowly added in portions such that the temperature
  2. customdoes not rise above 0° C
  3. additionAfter completion of the addition
  4. additionThe dark purple mixture is poured onto water (300 mL)
  5. extractionextracted twice with EA (300 mL)
  6. washThe organic extracts are washed with sat. aq. NaHCO3, 0.5 N aq. HCl
  7. customevaporated
  8. filtrationfiltered off
  9. washwashed with additional diethyl ether
  10. customdried under high vacuum

出典と根拠

ORDレコード
ord-56994b97fd3d4d8780cb7480791f0e2f
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08524752B2

反応ノート

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