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Ammonium dithiocarbamate → HCID 178433563, 화합물

HRID 973487
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HRID 973487 반응식
Br[CH:2]([C:6]1[CH:13]=[CH:12][C:9]([C:10]#[N:11])=[CH:8][CH:7]=1)[C:3](=O)[CH3:4].[C:14](=[S:17])([S-:16])[NH2:15].[NH4+]>C(O)C.O>[C:10]([C:9]1[CH:12]=[CH:13][C:6]([C:2]2[S:16][C:14]([SH:17])=[N:15][C:3]=2[CH3:4])=[CH:7][CH:8]=1)#[N:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11083854Ammonium dithiocarbamateHCID 15005405HCID 15005405, 화합물

생성물 1

HCID 178433563HCID 178433563, 화합물수율 26%

시약·촉매·용매 2

HCID 702Ethanol용매2회HCID 962Water용매

실험 절차

A solution of 4-(1-bromo-2-oxopropyl)benzonitrile (4.65 g, 0.02 mol) in absolute ethanol (20 ml) was added over 10 minutes to a stirred suspension of ammonium dithiocarbamate (2.2 g, 0.02 mol) in absolute ethanol (20 ml) at ambient temperature and the reaction mixture stirred for an additional 24 hours. The reaction mixture was then diluted with H2O (50 ml), the bulk of the ethanol evaporated under reduced pressure and product extracted with ethyl acetate. The organic extract was dried (MgSO4), filtered and the filtrate concentrated in vacuo. Trituration of the residue with ethanol and filtration gave the title product (1.2 g, 26%).

후처리

  1. customthe bulk of the ethanol evaporated under reduced pressure and product
  2. extractionextracted with ethyl acetate
  3. extractionThe organic extract
  4. dry with materialwas dried (MgSO4)
  5. filtrationfiltered
  6. concentrationthe filtrate concentrated in vacuo
  7. filtrationTrituration of the residue with ethanol and filtration

출처 및 근거

ORD 기록
ord-fd8e2d600ff64c178e383251f939fe8d
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05063237

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