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2-Mercaptoethanol → 2-[[(4-Nitrophenyl)methyl]thio]ethanol

HRID 1362883
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HRID 1362883 반응식
[SH:1][CH2:2][CH2:3][OH:4].[N+:5]([C:8]1[CH:15]=[CH:14][C:11]([CH2:12]Br)=[CH:10][CH:9]=1)([O-:7])=[O:6].C([O-])([O-])=O.[K+].[K+]>CC(C)=O.C1OCCOCCOCCOCCOCCOC1>[N+:5]([C:8]1[CH:15]=[CH:14][C:11]([CH2:12][S:1][CH2:2][CH2:3][OH:4])=[CH:10][CH:9]=1)([O-:7])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 15672-MercaptoethanolHCID 11430Potassium CarbonateHCID 660114-Nitrobenzyl bromide

생성물 1

HCID 135682062-[[(4-Nitrophenyl)methyl]thio]ethanol수율 119.3%

시약·촉매·용매 2

HCID 2855718-Crown-6촉매HCID 180Acetone용매

실험 절차

β-Mercaptoethanol (3.3 mL, 47.2 mmol) was added to a suspension of 4-nitrobenzyl bromide (10.0 g, 46.3 mmol), K2CO3 (16.1 g, 116.5 mmol), KI (154 mg, 0.9 mmol), and 18-crown-6 (258 mg, 1.0 mmol) in acetone (105 mL). The mixture was refluxed under N2 for 1.5 h, cooled to room temperature, filtered through a pad of celite, and concentrated in vacuo. The filtrate was poured into water (100 mL) and extracted with Et2O (2×100 mL). The extracts were washed with brine (150 mL), dried over Na2SO4, filtered, and concentrated in vacuo to give an orange oil (11.78 g), which was used in the following step without purification. MS: M(C9H11NO3S)=213.26, (M−OH)+=196.0.

후처리

  1. temperatureThe mixture was refluxed under N2 for 1.5 h
  2. filtrationfiltered through a pad of celite
  3. concentrationconcentrated in vacuo
  4. additionThe filtrate was poured into water (100 mL)
  5. extractionextracted with Et2O (2×100 mL)
  6. washThe extracts were washed with brine (150 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-32e3c75c7aed4e02ba24e57c8a92b97a
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07884098B2

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