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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → 4,4-dimethyl-3,4-dihydro-2H-thiochromene-6-carbaldehyde 1-oxide

HRID 402811
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HRID 402811 반응식
[CH3:1][C:2]1([CH3:14])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH:12]=[O:13])[CH:10]=2)[S:5][CH2:4][CH2:3]1.C1C=C(Cl)C=C(C(OO)=[O:23])C=1>ClCCl>[CH3:1][C:2]1([CH3:14])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH:12]=[O:13])[CH:10]=2)[S:5](=[O:23])[CH2:4][CH2:3]1
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 152843084,4-dimethyl-3,4-dihydro-2H-thiochromene-6-carbaldehyde

생성물 1

HCID 866852694,4-dimethyl-3,4-dihydro-2H-thiochromene-6-carbaldehyde 1-oxide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

4,4-Dimethyl-3,4-dihydro-2H-thiochromene-6-carbaldehyde (449 mg, 2.18 mmol, Example 5-28, Step 2) was dissolved in dichloromethane (22.0 mL) and mCPBA (751 mg, 4.35 mmol) was added in one portion. The reaction mixture was stirred at room temperature for 30 minutes. The mixture was then diluted with dichloromethane, washed with saturated aqueous NaHCO3, saturated aqueous NaCl, dried over Na2SO4, filtered and concentrated under vacuum. The crude mixture was purified by silica gel chromatography eluting with 0-5% MeOH/dichloromethane to afford the desired product as a colorless oil.

후처리

  1. washwashed with saturated aqueous NaHCO3, saturated aqueous NaCl
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated under vacuum
  5. customThe crude mixture was purified by silica gel chromatography
  6. washeluting with 0-5% MeOH/dichloromethane

출처 및 근거

ORD 기록
ord-197c1b7920374bb1a1e4e23e2dcca3ce
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08742110B2

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