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Tetrahydrofuran → 1-(Methanesulfinyl)-1-(methylsulfanyl)cyclopentane

HRID 329259
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HRID 329259 반응식
[CH3:1][S:2][CH2:3][S:4](=[O:6])[CH3:5].O1[CH2:11][CH2:10][CH2:9][CH2:8]1.[H-].[Na+].BrCCCCBr>C(Cl)Cl>[CH3:1][S:2][C:3]1([S:4](=[O:6])[CH3:5])[CH2:11][CH2:10][CH2:9][CH2:8]1
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참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 80561,4-DibromobutaneHCID 24758Sodium hydrideHCID 99129Methyl (methylsulfinyl)methyl sulfide

생성물 1

HCID 132987881-(Methanesulfinyl)-1-(methylsulfanyl)cyclopentane수율 46%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Formaldehyde dimethyl mercaptal S-oxide (1.49g) was dissolved in 15 ml. of tetrahydrofuran, and with ice cooling, 665 mg of sodium hydride was added. The mixture was stirred for 30 minutes with ice cooling, and then 2.936g of 1,4-dibromobutane was added. The mixture was stirred for 1 hour with ice cooling, for 24 hours at room temperature, and then for 44.5 hours at 50° C. Then, 100 ml. of methylene chloride was added, and the insoluble matter was separated. The filtrate was concentrated at reduced pressure, and the residue was separated by column chromatography (silica gel, eluted with 20% AcOEt-CH2Cl2, AcOEt, and MeOH) to afford 985 mg of cyclopentanone dimethyl mercaptal S-oxide. Also, 463 mg of formaldehyde dimethyl mercaptal S-oxide was recovered. The yield was 46%, and the conversion was 67%.

후처리

  1. stirringThe mixture was stirred for 1 hour with ice cooling, for 24 hours at room temperature
  2. waitfor 44.5 hours at 50° C
  3. customthe insoluble matter was separated
  4. concentrationThe filtrate was concentrated at reduced pressure
  5. customthe residue was separated by column chromatography (silica gel, eluted with 20% AcOEt-CH2Cl2, AcOEt, and MeOH)

출처 및 근거

ORD 기록
ord-0507fd2d980b4d7991a3851a7cc23a0e
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04020171

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