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Hydrochloric Acid → Thieno(2,3-b)pyridine

HRID 876783
ノート
印刷プレビュー

反応式

HRID 876783 の反応式
[N+:1]([C:4]1[S:5][CH:6]=[CH:7][CH:8]=1)([O-])=O.Cl.[Sn].CCO[CH:14](OCC)[CH2:15][CH:16](OCC)OCC.N.O>CCO.[Cl-].[Cl-].[Zn+2]>[S:5]1[C:4]2=[N:1][CH:14]=[CH:15][CH:16]=[C:8]2[CH:7]=[CH:6]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

8

反応物 5

HCID 313Hydrochloric AcidHCID 11866Thiophene, 2-nitro-HCID 671471,1,3,3-TetraethoxypropaneHCID 5352426Tin atom2 回HCID 12896473Azane;hydrate

生成物 1

HCID 289928Thieno(2,3-b)pyridine

試薬・触媒・溶媒 2

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート
HCID 3007855
Zincchloride
触媒
HCID 702Ethanol溶媒2 回

反応条件

温度
85 °C

実験手順

To a vigorously stirred mixture of 2-nitrothiophene (J-1) (13 g, 0.1 mol) and concentrated hydrochloric acid (195 mL) was added tin (25 g) at 0° C. After most of the tin was dissolved, EtOH (70 mL) and anhydrous ZnCl2 (6 g) were added. The mixture was heated to 85° C., and then treated with malonaldehyde bis(diethyl acetal) (17.2 g, 0.078 mol) in EtOH (30 mL). The resulting reaction was maintained at 85° C. for 1 h, then poured onto ice (100 g), basified with NH3.H2O, and extracted with DCM (75 mL×3). The combined organic layers were concentrated and purified by chromatography on silica gel to give the title compound. MS (m/z): 135 (M)+.

後処理

  1. customThe resulting reaction
  2. temperaturewas maintained at 85° C. for 1 h
  3. additionpoured onto ice (100 g)
  4. extractionextracted with DCM (75 mL×3)
  5. concentrationThe combined organic layers were concentrated
  6. custompurified by chromatography on silica gel

出典と根拠

ORDレコード
ord-59cd0608282f4ffc97ada4ac6792a908
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987269B2

反応ノート

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