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Acetone → 2,3:4,5-Di-o-isopropylidene-beta-D-fructopyranose

HRID 1576497
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인쇄 미리보기

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HRID 1576497 반응식
[OH:1][CH2:2][C:3]([C@H:5]([C@@H:7]([C@@H:9]([CH2:11][OH:12])[OH:10])[OH:8])[OH:6])=[O:4].[CH3:13][C:14]([CH3:16])=O.[CH3:17][CH2:18][CH2:19]CC>O>[CH3:13][C:14]1([CH3:16])[O:6][C@@H:5]2[C@@H:3]([CH2:2][O:1][C@@:9]3([CH2:11][OH:12])[O:10][C:18]([CH3:19])([CH3:17])[O:8][C@H:7]32)[O:4]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 5984D-(-)-FructoseHCID 8003Pentane

생성물 1

HCID 102443452,3:4,5-Di-o-isopropylidene-beta-D-fructopyranose

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

A mixture of 200 grams of D-fructose, 2 liters of acetone, 2 liters of pentane and 8 grams of ferric chloride is stirred and heated to reflux temperature. The reaction water is condensed and removed using a Dean-Stark type water separator. After the theoretical amount of water is removed, the mixture is cooled to 0°C., neutralized with 7 grams of sodium hydroxide in 10 milliliters of water and filtered. The filtrate is treated with 10 grams Norite SG, refiltered, and then concentrated to a syrup which is crystallized from ether-pentane to give 164.4 grams of product, m.p. 94°-95°C.

후처리

  1. temperatureheated
  2. temperatureto reflux temperature
  3. customcondensed
  4. customremoved
  5. customAfter the theoretical amount of water is removed
  6. filtrationfiltered
  7. additionThe filtrate is treated with 10 grams Norite SG
  8. concentrationconcentrated to a syrup which
  9. customis crystallized from ether-pentane

출처 및 근거

ORD 기록
ord-d1c1518a25a84121af1582eb7cf80e97
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03981860

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