ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Triethylamine → Methyl 3-Isocyanatothiophene-2-Carboxylate

HRID 1870532
ノート
印刷プレビュー

反応式

HRID 1870532 の反応式
[O:1]=[C:2](Cl)OC(Cl)(Cl)Cl.[NH2:9][C:10]1[CH:14]=[CH:13][S:12][C:11]=1[C:15]([O:17][CH3:18])=[O:16].C(N(CC)CC)C>O1CCOCC1>[N:9]([C:10]1[CH:14]=[CH:13][S:12][C:11]=1[C:15]([O:17][CH3:18])=[O:16])=[C:2]=[O: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 8471TriethylamineHCID 10426DiphosgeneHCID 89652Methyl 3-amino-2-thiophenecarboxylate

生成物 1

HCID 18696616Methyl 3-Isocyanatothiophene-2-Carboxylate

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

Diphosgene (4.6 mL) was added dropwise to a solution of methyl 3-amino-2-thiophenecarboxylate (5.0 g) in p-dioxane (100 mL) at room temperature under N2. Triethylamine (5.3 mL) was then added with concomitant formation of a white precipitate. The resulting reaction mixture was heated at reflux overnight. The reaction was allowed to cool to room temperature and then filtered to remove solid impurities. The precipitate was rinsed with diethyl ether (about 250 mL) and the filtrate was concentrated under reduced pressure to yield 6.4 g of crude title compound of Step A as a brown solid. 1H NMR (CDCl3): δ 7.43 (d,1H), 6.78 (d,1H), 3.92 (s,3H).

後処理

  1. customThe resulting reaction mixture
  2. temperaturewas heated
  3. temperatureat reflux overnight
  4. filtrationfiltered
  5. customto remove solid impurities
  6. washThe precipitate was rinsed with diethyl ether (about 250 mL)
  7. concentrationthe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-cfab7b1c4a6843019e0cb39045efbcef
出典データセット
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06096895

反応ノート

読み込み中…

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