2-Pentanone, 5-chloro- → 2-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dione

HRID 324597

반응식

HRID 324597 반응식
[C:1]1(=[O:11])[NH:5][C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[K].Cl[CH2:14][CH2:15][CH2:16][C:17](=[O:19])[CH3:18]>CN(C=O)C>[O:19]=[C:17]([CH3:18])[CH2:16][CH2:15][CH2:14][N:5]1[C:1](=[O:11])[C:2]2[C:3](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4]1=[O:6]

참가 물질

4

반응물 2

HCID 799932-Pentanone, 5-chloro-HCID 24194345Phthalimide potassium salt

생성물 1

HCID 2362702-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dione수율 34.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
60 °C

실험 절차

24.59 g (132.8 mmol) of potassium phthalimide are added to a solution of 14.3 ml (124.4 mmol) of 5-chloro-2-pentanone in 100 ml of DMF and the mixture is left to stir at room temperature for 3 h and at 60° C. for 30 h. After filtering, the filtrate is partitioned between water and dichloromethane. The phases are separated and the organic phase is washed successively with water, twice with an 0.2N solution of NaOH and water and then dried over sodium sulfate. After filtering, the solvent is removed in vacuo and the residue is chromatographed through silica gel using heptane/ethyl acetate=6/4. 9.8 g (34%) of (14.1) are obtained after concentrating the product fractions.

후처리

  1. waitthe mixture is left
  2. filtrationAfter filtering
  3. customthe filtrate is partitioned between water and dichloromethane
  4. customThe phases are separated
  5. washthe organic phase is washed successively with water, twice with an 0.2N solution of NaOH and water
  6. dry with materialdried over sodium sulfate
  7. filtrationAfter filtering
  8. customthe solvent is removed in vacuo
  9. customthe residue is chromatographed through silica gel

출처 및 근거

ORD 기록
ord-27b91a525a8f4762a5363865f4505b8c
출처 데이터셋
uspto-grants-2001_04
특허 번호
US06218415B1

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