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

Dabco → HCID 86660140、化合物

HRID 1746228
ノート
印刷プレビュー

反応式

HRID 1746228 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([OH:8])[C:3]=1[C:9](=[O:11])[CH3:10].[CH3:12][N:13]([CH3:17])[C:14](Cl)=[S:15].C1N2CCN(CC2)C1>CN(C=O)C>[C:9]([C:3]1[C:2]([F:1])=[CH:7][CH:6]=[CH:5][C:4]=1[O:8][C:14](=[S:15])[N:13]([CH3:17])[CH3:12])(=[O:11])[CH3:10]
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 9237DabcoHCID 27871Dimethylthiocarbamoyl chlorideHCID 27373242'-Fluoro-6'-hydroxyacetophenone

生成物 1

HCID 86660140HCID 86660140、化合物収率 74.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

1-(2-Fluoro-6-hydroxy-phenyl)-ethanone (2.5 g, 16.22 mmol) (available from Apollo Scientific) was dissolved in anhydrous DMF (20 mL.) Dimethylthiocarbamoyl chloride (2.2 g, 17.84 mmol) and DABCO (2.0 g, 17.84 mmol) were added sequentially in one portion. The reaction was permitted to stir overnight at ambient temperature. The reaction was quenched by pouring it into a mixture of 1N HCl-ice. The oily residue was extracted with dichloromethane and dried over sodium sulfate. The crude residue was purified by SGC (20% ethyl acetate in hexanes) to provide the title compound (2.93 g.) 1H NMR (200 MHz, CDCl3): δ (ppm)=7.407 (dd, 1H), 7.026 (t, 1H), 6.876 (d, 1H), 3.404 (s, 3H), 3.341 (sd, 3H), 2.58 (d, 3H).

後処理

  1. additionwere added sequentially in one portion
  2. customThe reaction was quenched
  3. additionby pouring it
  4. additioninto a mixture of 1N HCl-ice
  5. extractionThe oily residue was extracted with dichloromethane
  6. dry with materialdried over sodium sulfate
  7. customThe crude residue was purified by SGC (20% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-ba69be049e5045a5a4a0e703f5c5db19
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09149476B2

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