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2-Pentanone, 5-chloro- → HCID 178514990, 화합물

HRID 914289
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HRID 914289 반응식
Br[CH2:2][C:3](=O)[CH2:4][CH2:5][CH2:6][N:7]1[C:15](=[O:16])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]1=[O:17].ClCCCC(=O)C.C1(=O)NC(=O)C2=CC=CC=C12.[K].[C:38](=[S:41])([S-:40])[NH2:39].[NH4+]>C(O)C>[SH:41][C:38]1[S:40][CH:2]=[C:3]([CH2:4][CH2:5][CH2:6][N:7]2[C:15](=[O:16])[C:14]3=[CH:13][CH:12]=[CH:11][CH:10]=[C:9]3[C:8]2=[O:17])[N:39]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 799932-Pentanone, 5-chloro-HCID 11083854Ammonium dithiocarbamateHCID 139032932-(5-bromo-4-oxopentyl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 24194345Phthalimide potassium salt

생성물 1

HCID 178514990HCID 178514990, 화합물수율 57.8%

시약·촉매·용매 1

HCID 702
Ethanol
용매

실험 절차

2-(5-Bromo-4-oxopentyl)-isoindoline-1,3-dione (17.8 g) synthesized using 1-chloro-4-oxopentane and potassium phthalimide as starting materials and in reference to non-patent reference [Pharmazie, 47, 86 (1992)] and the like and ammonium dithiocarbamate (6.96 g) were suspended in ethanol (250 mL), and the suspension was refluxed for 6 hr. The precipitated crystals were collected by filtration and washed with ethanol to give the title compound (10.1 g) as white crystals.

후처리

  1. temperaturethe suspension was refluxed for 6 hr
  2. filtrationThe precipitated crystals were collected by filtration
  3. washwashed with ethanol

출처 및 근거

ORD 기록
ord-27f5b5851b9844908805bcf24ccc8608
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08026370B2

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