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Water → 1-(Methanesulfonylmethyl)-3-nitrobenzene

HRID 514693
ノート
印刷プレビュー

反応式

HRID 514693 の反応式
ClC1C=C(C(OO)=[O:9])C=CC=1.[CH3:12][S:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[CH:16]=1.C(=O)(O)[O-].[Na+].[OH2:29]>C(Cl)Cl>[CH3:12][S:13]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[CH:16]=1)(=[O:9])=[O:29]
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

6

反応物 4

HCID 962WaterHCID 70297m-Chloroperbenzoic acidHCID 516892Sodium BicarbonateHCID 22031873Methyl(3-nitrobenzyl)sulfane

生成物 1

HCID 179084331-(Methanesulfonylmethyl)-3-nitrobenzene

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

3-Chlorobenzenecarboperoxoic acid (77%; 26.9 g; 120 mmol) was added to a stirred solution of 1-[(methylsulfanyl)methyl]-3-nitrobenzene (10.0 g) in DCM (1305 mL) at 0° C. The batch was stirred at 0° C. for 30 minutes and then 2.5 hours at room temperature. The batch was diluted with water (300 mL) before sodium bicarbonate (11.0 g) was added. The batch was extracted with DCM (2×). The combined organic phases were filtered using a Whatman filter and concentrated. The residue was purified by chromatography (DCM/ethanol 95:5) and finally recrystallized from ethyl acetate to give the desired product (6.2 g; 28.9 mmol).

後処理

  1. custom2.5 hours
  2. customat room temperature
  3. additionwas added
  4. extractionThe batch was extracted with DCM (2×)
  5. filtrationThe combined organic phases were filtered
  6. filtrationfilter
  7. concentrationconcentrated
  8. customThe residue was purified by chromatography (DCM/ethanol 95:5)
  9. customfinally recrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-5a2723e22f674246a963491f0d427b08
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09108926B2

反応ノート

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