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Dibromomethane → 2-(p-Chlorophenoxymethylimino)-1,3-dithietane

HRID 436629
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HRID 436629 반응식
C(Br)Br.[CH2:4](N(CC)CC)C.[Cl:11][C:12]1[CH:23]=[CH:22][C:15]([O:16][CH2:17][NH:18][C:19](=[S:21])[S-:20])=[CH:14][CH:13]=1.[K+].S1CCS1>O.CN(C)C=O>[Cl:11][C:12]1[CH:23]=[CH:22][C:15]([O:16][CH2:17][N:18]=[C:19]2[S:20][CH2:4][S:21]2)=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 3024DibromomethaneHCID 8471TriethylamineHCID 123092831,2-DithietaneHCID 23667330Potassium p-chlorophenoxymethyldithiocarbamate

생성물 1

HCID 214532822-(p-Chlorophenoxymethylimino)-1,3-dithietane

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

To a mixture of 19.3 g. of methylene bromide and 3.7 g. of triethylamine in 100 ml. of dimethylformamide was added 10.0 g. of potassium p-chlorophenoxymethyldithiocarbamate in portions. After one to two hours, the mixture was poured into water and partitioned into ethylene chloride. The dried ethylene chloride mixture was saturated with dry hydrogen chloride and the resulting salt collected by filtration. Hydrolysis of the salt in a chloroform-water mixture followed by separation, drying and concentration of the chloroform layer gave 3.5 g. of the dithietane as pale yellow crystals, m.p. 64.5°-66.0° C.

후처리

  1. additionTo a mixture of 19.3 g
  2. waitAfter one to two hours
  3. custompartitioned into ethylene chloride
  4. filtrationthe resulting salt collected by filtration
  5. customHydrolysis of the salt in a chloroform-water mixture
  6. customfollowed by separation
  7. customdrying
  8. customconcentration of the chloroform layer gave 3.5 g

출처 및 근거

ORD 기록
ord-04f2db9f073a4161aed49e48dc89dc23
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04009279

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