Triethylsilane → 3-Methyl-6-(2-bromoethyl)benzothiazolinone

HRID 1614215ノート

反応式

HRID 1614215 の反応式
[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([C:11](=O)[CH2:12][Br:13])=[CH:10][C:5]=2[S:4](=[O:15])[CH2:3]1.C([SiH](CC)CC)C>FC(F)(F)C(O)=O>[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][CH2:12][Br:13])=[CH:10][C:5]=2[S:4](=[O:15])[CH2:3]1

参加物

4

反応物 2

HCID 12052TriethylsilaneHCID 867466573-Methyl-6-(bromoacetyl)benzothiazolinone

生成物 1

HCID 701838363-Methyl-6-(2-bromoethyl)benzothiazolinone

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

In a 500-cm3 ground-necked flask surmounted by a condenser and placed in an oil bath, 42.9 g (0.15 mol) of 3-methyl-6-(bromoacetyl)benzothiazolinone are dissolved in 77 cm3 of trifluoroacetic acid with magnetic stirring and while the temperature is stabilized at 60° C. 52.7 cm3 (0.33 mol) of triethylsilane are introduced dropwise via a dropping funnel. After the addition, the heating is stopped and the mixture is left stirring vigorously for 30 hours. The reaction medium is hydrolyzed by pouring it into ice-cold water, and the precipitate obtained is drained and washed with water until the filtrate is neutral and then with hexane. The product is dried and recrystallized in cyclohexane.

後処理

  1. customIn a 500-cm3 ground-necked flask surmounted by a condenser
  2. customplaced in an oil bath
  3. customis stabilized at 60° C
  4. additionAfter the addition
  5. waitthe mixture is left
  6. stirringstirring vigorously for 30 hours
  7. additionby pouring it into ice-cold water
  8. customthe precipitate obtained
  9. washwashed with water until the filtrate
  10. customThe product is dried
  11. customrecrystallized in cyclohexane

出典と根拠

ORDレコード
ord-83351ddc49854ae5b96bd59c7e7c7319
出典データセット
uspto-grants-1993_03
特許番号
US05196434

反応ノート

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