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Benzocaine → Ethyl 4-[3-(trimethylsilyl)propylamino]benzoate

HRID 652016
ノート
印刷プレビュー

反応式

HRID 652016 の反応式
[CH3:1][Si:2]([CH3:8])([CH3:7])[CH2:3][CH2:4][CH2:5]Br.[NH2:9][C:10]1[CH:20]=[CH:19][C:13]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:12][CH:11]=1>CN(C)P(N(C)C)(N(C)C)=O>[CH3:1][Si:2]([CH3:8])([CH3:7])[CH2:3][CH2:4][CH2:5][NH:9][C:10]1[CH:11]=[CH:12][C:13]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:19][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2337BenzocaineHCID 128458003-Bromopropyltrimethylsilane

生成物 1

HCID 13884861Ethyl 4-[3-(trimethylsilyl)propylamino]benzoate

試薬・触媒・溶媒 1

HCID 12679Hexamethylphosphoramide溶媒

実験手順

A solution of 20 g. 3-(trimethylsilyl)propyl bromide and 33.9 g. ethyl 4-aminobenzoate in 75 ml. hexamethylphosphoramide was stirred at 100° for 18 hr. The cooled reaction was diluted with 100 ml. water, the layers were separated, and the aqueous layer was washed three times 100 ml. portions of methylene chloride. The combined organic solutions were washed with water and brine, dried with anhydrous magnesium sulfate, passed through a pad of hydrous magnesium silicate, and evaporated to 96 g. orange liquid. The liquid was dissolved into 100 ml. ethanol and the product was precipitated with 100 ml. water. The solid was filtered and dried. Crystallization from water-ethanol yielded the title compound as a white solid, m.p. 64°-66° C.

後処理

  1. customThe cooled reaction
  2. additionwas diluted with 100 ml
  3. customwater, the layers were separated
  4. washthe aqueous layer was washed three times 100 ml
  5. washThe combined organic solutions were washed with water and brine
  6. dry with materialdried with anhydrous magnesium sulfate
  7. customevaporated to 96 g
  8. dissolutionThe liquid was dissolved into 100 ml
  9. customethanol and the product was precipitated with 100 ml
  10. filtrationThe solid was filtered
  11. customdried
  12. customCrystallization from water-ethanol

出典と根拠

ORDレコード
ord-91cbab4506ef4d86b9ba3a4c19b0dea6
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04670421

反応ノート

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