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Methanol → HCID 86739629, 화합물

HRID 2418018
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HRID 2418018 반응식
CO[CH:3]=[CH:4][C:5](=[O:7])[CH3:6].[C:8]([O-])([O-])=[O:9].[K+].[K+].CO.[CH3:16][O:17][CH:18]([O:21][CH3:22])[CH2:19][SH:20]>O1CCCC1.CCOCC.O>[CH3:16][O:17][C:18]([O:9][CH3:8])([O:21][CH3:22])[CH2:19][S:20][CH2:3][CH2:4][C:5](=[O:7])[CH3:6]
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참가 물질

7

반응물 4

HCID 887MethanolHCID 11430Potassium CarbonateHCID 942973-Buten-2-one, 4-methoxy-HCID 148182602,2-Dimethoxyethane-1-thiol

생성물 1

HCID 86739629HCID 86739629, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 21868444
Ether tetrahydrofuran
용매

실험 절차

To a solution of 2.3 g. (18.9 mmol) of 4-methoxy-3-buten-2-one and 50 mg. K2CO3 in 15 ml. of methanol was added 1.88 g. (18.9 mmol) of 2-mercaptoacetaldehyde dimethyl acetal and the reaction mixture heated to reflux for 10 minutes. On cooling, the methanol was removed by rotatory evaporation, 25 ml. of ether was added and the solution was extracted with water, brine, and dried over anhydrous magnesium sulfate. Filtration and removal of solvent afforded 2.95 g. (70%) of water white oil homogeneous by TLC (SiO2), tetrahydrofuran/ether, 1:1; Mol. dist. 140° (0.2 mm Hg), 1H-NMR (CDCl3) delta 2.21 (s, 3), 2.66-3.11 (m, 4), 3.42 (s, 9), 4.44 (t, 1), 4.89 (doublet of doublets, 1); IR (film) cm-1 1710 (s).

후처리

  1. temperatureto reflux for 10 minutes
  2. temperatureOn cooling
  3. customthe methanol was removed by rotatory evaporation, 25 ml
  4. additionof ether was added
  5. extractionthe solution was extracted with water, brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationFiltration and removal of solvent
  8. customafforded 2.95 g
  9. custom140° (0.2 mm Hg), 1H-NMR (CDCl3) delta 2.21 (s, 3), 2.66-3.11 (m, 4), 3.42 (s, 9), 4.44 (t, 1), 4.89 (doublet of doublets, 1)

출처 및 근거

ORD 기록
ord-1276ec8c354a40cf8f8146702bf9a8c3
출처 데이터셋
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04471139

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