Chloroform → 2-Chloro-4,5,6,7-tetrahydro-1-benzothiophen-4-amine

HRID 263191ノート

反応式

HRID 263191 の反応式
Cl.[S:2]1[CH:6]=[CH:5][C:4]2[CH:7]([NH2:11])[CH2:8][CH2:9][CH2:10][C:3]1=2.C(Cl)(Cl)[Cl:13].S(Cl)(Cl)(=O)=O.[OH-].[Na+]>O>[Cl:13][C:6]1[S:2][C:3]2[CH2:10][CH2:9][CH2:8][CH:7]([NH2:11])[C:4]=2[CH:5]=1

参加物

6

反応物 4

HCID 6212ChloroformHCID 14798Sodium HydroxideHCID 24648Sulfuryl chlorideHCID 173886004,5,6,7-Tetrahydrobenzo[b]thiophen-4-amine hydrochloride

生成物 1

HCID 203489752-Chloro-4,5,6,7-tetrahydro-1-benzothiophen-4-amine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A sample of 11.4 grams 4,5,6,7-tetrahydrobenzo[b]thiophen-4-amine hydrochloride is stirred in 150 ml. of chloroform at about 10° C., and 6.1 ml. of sulfuryl chloride is added dropwise. The mixture is stirred for 3.5 hours at room temperature, and then about 20 ml. of 50% sodium hydroxide solution is added gradually to dissolve the suspended solid. The mixture is then poured into water and extracted with chloroform twice. The extracts are dried, evaporated to dryness, and the residue is distilled to give 7.4 grams of 2-chloro-4,5,6,7-tetrahydrobenzo[b]thiophen-4-amine, boiling point 94° C. to 98° C./0.5 Torr.

後処理

  1. customat about 10° C.
  2. dissolutionto dissolve the suspended solid
  3. extractionextracted with chloroform twice
  4. customThe extracts are dried
  5. customevaporated to dryness
  6. distillationthe residue is distilled

出典と根拠

ORDレコード
ord-d8b10acc7c244552be108a24fe2008f7
出典データセット
uspto-grants-1979_05
特許番号
US04156670

反応ノート

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