Hydrochloric Acid → 5-(2-nitroethyl)-1H-indole

HRID 343902ノート

反応式

HRID 343902 の反応式
[BH4-].[Na+].[OH-].[Na+].[N+:5]([CH:8]=[CH:9][C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[NH:15][CH:14]=[CH:13]2)([O-:7])=[O:6].Cl>C(#N)C.O>[N+:5]([CH2:8][CH2:9][C:10]1[CH:11]=[C:12]2[C:16](=[CH:17][CH:18]=1)[NH:15][CH:14]=[CH:13]2)([O-:7])=[O:6]

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 544650165-(2-nitro-vinyl)-1H-indole

生成物 1

HCID 131097235-(2-nitroethyl)-1H-indole収率 40.6%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6342Acetonitrile溶媒

反応条件

温度
0 °C

実験手順

A solution of sodium borohydride (2.0 g) and 40% w/v aqu. NaOH was added dropwise to a solution of the the product from step (b) (1.9 g) in acetonitrile (55 ml) at 0° C. The pH was maintained at 3-6 by periodic additions of 2N aqu. HCl. The resulting solution was stirred at 0° C. for 2 hours, then diluted with water and extracted with DCM. The combined extracts were washed with brine, dried and evaporated in vacuo to give a yellow oil which was eluted through a silica column using chloroform as eluant to give the desired product as a pale yellow oil (0.78 g).

後処理

  1. temperatureThe pH was maintained at 3-6 by periodic additions of 2N aqu
  2. extractionextracted with DCM
  3. washThe combined extracts were washed with brine
  4. customdried
  5. customevaporated in vacuo
  6. customto give a yellow oil which
  7. washwas eluted through a silica column

出典と根拠

ORDレコード
ord-957ef5114f7b49c881c07499aaedd00a
出典データセット
uspto-grants-1999_01
特許番号
US05863935

反応ノート

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