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Sodium Methoxide → (2,6-Dibromo-4-fluoro-phenyl)-thiourea

HRID 1521426
ノート
印刷プレビュー

反応式

HRID 1521426 の反応式
C([NH:9][C:10]([NH:12][C:13]1[C:18]([Br:19])=[CH:17][C:16]([F:20])=[CH:15][C:14]=1[Br:21])=[S:11])(=O)C1C=CC=CC=1.C[O-].[Na+]>CO>[Br:19][C:18]1[CH:17]=[C:16]([F:20])[CH:15]=[C:14]([Br:21])[C:13]=1[NH:12][C:10]([NH2:9])=[S:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10942334Sodium MethoxideHCID 866512491-Benzoyl-3-(2,6-dibromo-4-fluoro-phenyl)-thiourea

生成物 1

HCID 86651250(2,6-Dibromo-4-fluoro-phenyl)-thiourea収率 100%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
23 °C

実験手順

To a solution of 1-benzoyl-3-(2,6-dibromo-4-fluoro-phenyl)-thiourea (1.37 g, 3.17 mmol) in MeOH (12 mL) was added dropwise a sodium methoxide solution (5.4M in MeOH, 1.29 mL, 6.96 mmol) at 0° C. The mixture was warmed to 23° C. and stirred for 16 hours. MeOH was concentrated under reduced pressure. The residue was dissolved in water, cooled to 0° C., and acidified to pH 4 with 1M HCl. The resulting precipitate was collected by filtration and washed with hexanes to yield titled compound (1.04 g, 99%). MS (ESI/CI): mass calcd. for C7H5Br2FN2S, 325.9; m/z found, 326.9 [M+H]+. 1H NMR (400 MHz, CD3OD-d4): 8.05-8.01 (m, 2H).

後処理

  1. concentrationMeOH was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in water
  3. temperaturecooled to 0° C.
  4. filtrationThe resulting precipitate was collected by filtration
  5. washwashed with hexanes

出典と根拠

ORDレコード
ord-94e460b2f01d48898d41318f07d93957
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073923B2

反応ノート

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