Isopropanol → N-(2-Chloroethyl)phthalimide

HRID 5272

반응식

HRID 5272 반응식
C(O)(C)C.[ClH:5].CNOC.Br[CH2:11][CH2:12][N:13]1[C:17](=[O:18])[C:16]2=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]2[C:14]1=[O:23].C(=O)(O)[O-].[Na+]>C(N(CC)CC)C>[Cl:5][CH2:11][CH2:12][N:13]1[C:17](=[O:18])[C:16]2=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]2[C:14]1=[O:23]

참가 물질

6

반응물 4

HCID 3776IsopropanolHCID 113251H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 81138Methanamine, N-methoxy-, hydrochloride (1:1)HCID 516892Sodium Bicarbonate

생성물 1

HCID 234274N-(2-Chloroethyl)phthalimide수율 65.4%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

To a suspension of 50 ml of isopropanol containing N,O-dimethylhydroxylamine hydrochloride (3.90 g, 40.0 mmol) was added dropwise 5.56 ml of triethylamine. The resulting mixture became homogeneous after 5 minutes. Thereto was added 2.45 g (10.0 mmol) of N-(bromoethyl)phthalimide and the mixture was refluxed for 29 hours. This was cooled to room temperature, then poured into 200 ml of a saturated aqueous solution of sodium bicarbonate and extracted with chloroform. The organic layer was separated and was washed with water and dried over magnesium sulfate. Chloroform was distilled off and the residue was purified by column chromatography on silica gel. Development with 30% hexane-chloroform resulted in elution of 1.37 g of N-(2-chloroethyl)-phthalimide and further development with chloroform resulted in 0.964 g (yield: 41%) of white cyrstals of N-[2-(N-methoxy-N-methylamino)ethyl]phthalimide.

후처리

  1. temperaturethe mixture was refluxed for 29 hours
  2. extractionextracted with chloroform
  3. customThe organic layer was separated
  4. washwas washed with water
  5. dry with materialdried over magnesium sulfate
  6. distillationChloroform was distilled off
  7. customthe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-e26bcea9d9b94655bfa1a6ada380e790
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05244487

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