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

HRID 1973578
ノート
印刷プレビュー

反応式

HRID 1973578 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒

実験手順

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 another 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.

後処理

  1. additionTo a mixture of 19.3 g
  2. waitAfter another 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

出典と根拠

ORDレコード
ord-839883dbabb94c898f7f946c3057c407
出典データセット
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03997668

反応ノート

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