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Sulfuric Acid → HCID 18406868, 화합물

HRID 1016401
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HRID 1016401 반응식
[OH:1][C:2]1[CH2:3][C:4](=[O:7])[O:5][CH:6]=1.[C:8](O)([CH3:11])([CH3:10])[CH3:9].S(=O)(=O)(O)O>O>[C:8]([CH:3]1[C:2]([OH:1])=[CH:6][O:5][C:4]1=[O:7])([CH3:11])([CH3:10])[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 6386tert-ButanolHCID 221728094-Hydroxyfuran-2(3H)-one

생성물 1

HCID 18406868HCID 18406868, 화합물수율 7.4%

시약·촉매·용매 1

HCID 962Water용매

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온도
40 °C

실험 절차

To 4-hydroxy-2-furanone (50 g, 0.5 mol) in tert-butanol (50 ml, 0.53 mol) was added concentrated sulfuric acid (25 ml). The mixture was heated at 40° C. for 20 h then allowed to cool. Water (250 ml) was added and the mixture was extracted with diethyl ether (3×250 ml), the diethyl ether layers were combined, washed with brine (250 ml), dried (Na2SO4), filtered and concentrated in vacuo to give a brown solid. The solid was purified by silica gel chromatography with 0%→100% ethyl acetate/isohexane as eluent followed by two recrystallisations from ethyl acetate/isohexane (1:1) to afford the required product (5.75 g). Data for the title compound: 1H NMR (400 MHz, DMSO) δ 1.21 (9H, s), 4.48 (2H, s), 11.40 (1H, s); MS (ES+) m/e 156 [MH]+.

후처리

  1. temperatureto cool
  2. extractionthe mixture was extracted with diethyl ether (3×250 ml)
  3. washwashed with brine (250 ml)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto give a brown solid
  8. customThe solid was purified by silica gel chromatography with 0%→100% ethyl acetate/isohexane as eluent
  9. customfollowed by two recrystallisations from ethyl acetate/isohexane (1:1)

출처 및 근거

ORD 기록
ord-d8fc069aa3d845b5aa2229d29154ee54
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06476030B1

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