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Dimethylformamide → 2-Chloro-5-nitrobenzo[d]oxazole

HRID 512450
ノート
印刷プレビュー

反応式

HRID 512450 の反応式
S[C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=2[N:6]=1.CN(C=O)C.S(Cl)([Cl:21])=O>>[Cl:21][C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=2[N:6]=1
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 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 178526504HCID 178526504、化合物

生成物 1

HCID 103527232-Chloro-5-nitrobenzo[d]oxazole

反応条件

温度
65 °C

実験手順

Subsequently, the crude 2-mercapto-5-nitrobenzoxazole (10 g, 51 mmol), previously prepared, was dissolved in thionyl chloride (100 mL). DMF (60 μL) was added and the reaction mixture was heated at 65° C. for 45 min. After cooling, the solvent was removed under reduced pressure and to the residue, toluene was added twice (2×20 mL) and each time subsequently evaporated in vacuo to remove volatiles via azeotrope. The resultant crude product was dissolved in ethyl acetate (400 mL), washed with brine (200 mL), dried over Na2SO4, filtered, and concentrated to give compound 29, 2-chloro-5-nitrobenzoxazole, as (8.2 g, crude).

後処理

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure and to the residue, toluene
  3. additionwas added twice (2×20 mL)
  4. customeach time subsequently evaporated in vacuo
  5. customto remove volatiles via azeotrope
  6. dissolutionThe resultant crude product was dissolved in ethyl acetate (400 mL)
  7. washwashed with brine (200 mL)
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-a8933e70a14844059ac74a47cc63921b
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09102636B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート