Methyl pyruvate → Methyl 2-Methyl-5,5-diphenyl[1,3]dioxane-2-carboxylate

HRID 1859757노트

반응식

HRID 1859757 반응식
[C:1]1([C:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)([CH2:10][OH:11])[CH2:8][OH:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:18]([O:23][CH3:24])(=[O:22])[C:19]([CH3:21])=O.O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O>>[CH3:21][C:19]1([C:18]([O:23][CH3:24])=[O:22])[O:9][CH2:8][C:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH2:10][O:11]1

참가 물질

4

실험 절차

A mixture of 22.8 g (0.1 M) of 2,2-diphenyl-1,3-propanediol and 100 g (0.98 M) of methyl pyruvate is brought to 70° C. in a 500 ml round-bottomed flask under a nitrogen atmosphere. 22.4 g (0.156 M) of P2O5 are added portionwise. An exothermic reaction takes place and the temperature rises to 98° C. The mixture is allowed to return to room temperature and is poured slowly into ice-cold water. This mixture is extracted with methylene chloride and the extracts are washed with sodium hydroxide and water. The extracts are concentrated and the residue is chromatographed by flash chromatography (70 CH2Cl2/50 cyclohexane eluent). The product is then recrystallized from 40 ml of diisopropyl ether. 7 g of a product of m.p. 116° C. are obtained.

후처리

  1. customis brought to 70° C. in a 500 ml round-bottomed flask under a nitrogen atmosphere
  2. customAn exothermic reaction
  3. customrises to 98° C
  4. customto return to room temperature
  5. additionis poured slowly into ice-cold water
  6. extractionThis mixture is extracted with methylene chloride
  7. washthe extracts are washed with sodium hydroxide and water
  8. concentrationThe extracts are concentrated
  9. customthe residue is chromatographed by flash chromatography (70 CH2Cl2/50 cyclohexane eluent)
  10. customThe product is then recrystallized from 40 ml of diisopropyl ether

출처 및 근거

ORD 기록
ord-d44e178896d34d1297817129dfb18f97
출처 데이터셋
uspto-grants-2003_03
특허 번호
US06528538B1

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