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Phosphoric Acid → 3-Chloro-4,5,6,7-tetrahydro-1,2-benzisothiazole

HRID 566458
ノート
印刷プレビュー

反応式

HRID 566458 の反応式
O[C:2]1[C:6]2[CH2:7][CH2:8][CH2:9][CH2:10][C:5]=2[S:4][N:3]=1.Cl.[NH+]1C=CC=CC=1.P(=O)(O)(O)O.P(Cl)(Cl)([Cl:25])=O>>[Cl:25][C:2]1[C:6]2[CH2:7][CH2:8][CH2:9][CH2:10][C:5]=2[S:4][N:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 1004Phosphoric AcidHCID 24813Phosphorus oxychlorideHCID 21584435Pyridinium hydrochlorideHCID 178519008HCID 178519008、化合物

生成物 1

HCID 107735623-Chloro-4,5,6,7-tetrahydro-1,2-benzisothiazole

反応条件

温度
90 °C

実験手順

A mixture of 3-hydroxy-4,5,6,7-tetrahydro-1,2-benzisothiazole 22a (4.74 g), pyridinium hydrochloride (12.7 g), phosphoric acid (2.1 g) and phosphorus oxychloride (25 mL) was stirred at 90 ° C. for 5 h. The reaction mixture was evaporated and ethyl acetate (130 mL) was added to the residue. A saturated solution of sodium hydrogencarbonate (130 mL) was added and after 10 min of stirring the phases were separated. The aqueous phase was extracted with ethyl acetate (2 x 150 mL) and the combined organic phases were dried and evaporated to give an oil. Column chromatography on silica gel (eluent: toluene-ethyl acetate 1:1) gave the title compound as a yellow oil (2.8 g).

後処理

  1. customThe reaction mixture was evaporated
  2. additionethyl acetate (130 mL) was added to the residue
  3. additionA saturated solution of sodium hydrogencarbonate (130 mL) was added and after 10 min
  4. stirringof stirring the phases
  5. customwere separated
  6. extractionThe aqueous phase was extracted with ethyl acetate (2 x 150 mL)
  7. customthe combined organic phases were dried
  8. customevaporated
  9. customto give an oil

出典と根拠

ORDレコード
ord-44f36ef58e62485ebce396187b21e920
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06174909B1

反応ノート

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