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Water → 1-(Methanesulfonylmethyl)-3-nitrobenzene

HRID 1405169
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인쇄 미리보기

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HRID 1405169 반응식
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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

HCID 179084331-(Methanesulfonylmethyl)-3-nitrobenzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

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 combinded 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)

후처리

  1. custom2.5 hours
  2. customat room temperature
  3. additionwas added
  4. extractionThe batch was extracted with DCM (2×)
  5. filtrationThe combinded 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

출처 및 근거

ORD 기록
ord-b3f5709b432f4b57aee928ad63ca5ae3
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916557B2

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