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Hydrochloric Acid → 3-Phenyl-2-benzamido-1-propanethiol

HRID 1856409
ノート
印刷プレビュー

反応式

HRID 1856409 の反応式
[C:1]1([CH2:7][CH:8]([NH:11][C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9]Cl)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.NC(N)=[S:22].[OH-].[Na+].Cl>C(O)C.O>[C:1]1([CH2:7][CH:8]([NH:11][C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9][SH:22])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=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 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 209006N-(1-Chloro-3-phenylpropan-2-yl)benzenecarboximidic acidHCID 2723790Thiourea

生成物 1

HCID 233449073-Phenyl-2-benzamido-1-propanethiol

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 962
Water
溶媒

実験手順

80.4 millimole (mm) of 3-phenyl-2-benzamido-1-chloropropane and 80.4 mm of thiourea are dissolved in 300 ml of ethanol. The resulting solution is refluxed for three hours. 6.7 g of sodium hydroxide is dissolved in 40 ml of water and is added under an inert atmosphere to the solution which is thereafter refluxed for an additional 21/2 hours. The solution is then cooled and acidified to pH 1 with 1 N HCl. The resulting mixture is then poured over ice to yield a precipitate which is collected by filtration and then dissolved in chloroform. The chloroform is dried with magnesium sulfate and then evaporated to yield the solid 3-phenyl-2-benzamido-1-propanethiol.

後処理

  1. temperatureThe resulting solution is refluxed for three hours
  2. additionis added under an inert atmosphere to the solution which
  3. temperatureis thereafter refluxed for an additional 21/2 hours
  4. temperatureThe solution is then cooled
  5. additionThe resulting mixture is then poured over ice
  6. customto yield a precipitate which
  7. filtrationis collected by filtration
  8. dissolutiondissolved in chloroform
  9. dry with materialThe chloroform is dried with magnesium sulfate
  10. customevaporated

出典と根拠

ORDレコード
ord-04a9c60c17ad4dd0a7e2682609dd8f0f
出典データセット
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04219497

反応ノート

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