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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 10846754, 화합물 → HCID 11041589, 화합물

HRID 1030035
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HRID 1030035 반응식
O[CH2:2][C:3]1([CH2:14][OH:15])[O:10][C@@H:7]([O:8]C)[C@H:6]([OH:11])[C@@H:5]([OH:12])[C@H:4]1[OH:13]>S(=O)(=O)(O)O>[OH:15][CH2:14][C@@:3]12[CH2:2][O:8][C@@H:7]([O:10]1)[C@H:6]([OH:11])[C@@H:5]([OH:12])[C@H:4]2[OH:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 10846754HCID 10846754, 화합물

생성물 1

HCID 11041589HCID 11041589, 화합물수율 39.6%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

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온도
100 °C

실험 절차

Methyl 5-C-hydroxymethyl-α-L-arabino-hexopyranoside (3) (59.0 g, 0.263 moles) is dissolved in 0.70M sulfuric acid (260 ml), and stirred at 100° C. for 90 minutes. The solution is cooled to room temperature and neutralized using an ion exchange resin (Amberlite IRA-400 (OH-), 250 ml). The filtrate is removed from the resin, and the filtrate is refluxed for 15 minutes with activated carbon (4.0 g). Carbon is removed with a glass fiber filter, and the filtrate is evaporated to dryness with ethanol. The white waxy residue is refluxed for 15 minutes with methanol (50 ml). The solution is stored overnight at 0° C. The product crystal are filtered to yield 20.0 g (39.6%) of 5-C-hydroxymethyl 1,6-anhydro-β-L-altropyranose (4). M.P.=166.5° C.-168.5° C. [α]D23 =+145.1 (7.2 c. in water)

후처리

  1. temperatureThe solution is cooled to room temperature
  2. customThe filtrate is removed from the resin
  3. temperaturethe filtrate is refluxed for 15 minutes with activated carbon (4.0 g)
  4. customCarbon is removed with a glass fiber
  5. filtrationfilter
  6. customthe filtrate is evaporated to dryness with ethanol
  7. temperatureThe white waxy residue is refluxed for 15 minutes with methanol (50 ml)
  8. waitThe solution is stored overnight at 0° C
  9. filtrationThe product crystal are filtered

출처 및 근거

ORD 기록
ord-654710d647f54d308ffe66b2672564c6
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05104797

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