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Methanol → HCID 13837141、化合物

HRID 2080016
ノート
印刷プレビュー

反応式

HRID 2080016 の反応式
CC(C)([O-])C.[K+].[N+:7]([C:10]1[S:11][CH:12]=[CH:13][CH:14]=1)([O-:9])=[O:8].[CH:15](Cl)([Cl:17])[Cl:16].CO>CN(C)C=O.[Cl-].[Na+].O.C(O)(=O)C>[Cl:16][CH:15]([Cl:17])[C:14]1[CH:13]=[CH:12][S:11][C:10]=1[N+:7]([O-:9])=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 887MethanolHCID 6212ChloroformHCID 11866Thiophene, 2-nitro-HCID 23665647Potassium tert-butoxide

生成物 1

HCID 13837141HCID 13837141、化合物収率 94%

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒
HCID 6228
Dimethylformamide
溶媒
2 回
HCID 57417360Sodium chloride; water溶媒

実験手順

To a solution of potassium tert-butoxide (23.0 mL, 1.0M tetrahydrofuran solution, 23.2 mmol) in N,N-dimethyl formamide (20 mL) were added a mixture solution of 2-nitro-thiophene (1.00 g, 7.74 mmol) in chloroform (682 μl, 8.51 mmol) and N,N-dimethylformamide (2 mL) dropwise at −78° C., the solution was stirred for 5 minutes, and then, methanol and acetic acid were added at 0° C. Brine was added to the reaction solution, which was then extracted with ethyl acetate. The solvent was evaporated in vacuo, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1), and the title compound (1.54 g, 7.26 mmol, 94%) was obtained as a light brown solid.

後処理

  1. extractionwas then extracted with ethyl acetate
  2. customThe solvent was evaporated in vacuo
  3. customthe residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1)

出典と根拠

ORDレコード
ord-1dddabca55764c5ba2d8b4d0e8d08205
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07932272B2

反応ノート

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