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Sodium borohydride → HCID 19875845、化合物

HRID 1886344
ノート
印刷プレビュー

反応式

HRID 1886344 の反応式
[CH3:1][CH:2]([CH3:18])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:14])[CH3:13])=[C:7]([N+:15]([O-:17])=[O:16])[CH:6]=1)=[O:4].[BH4-].[Na+]>CO>[OH:4][CH:3]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:14])[CH3:13])=[C:7]([N+:15]([O-:17])=[O:16])[CH:6]=1)[CH:2]([CH3:18])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 19875874HCID 19875874、化合物

生成物 1

HCID 19875845HCID 19875845、化合物収率 100%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a stirred and cooled (ice water, 10° C.) solution of 30 parts of intermediate 14, namely N-[4-(2-methyl-1-oxopropyl)-2-nitrophenyl]acetamide in 240 parts of methanol were added portionwise 4.5 parts of sodium tetrahydroborate. Upon completion, stirring was continued for 1 hour. The reaction mixture was evaporated and the residue was extracted with dichloromethane (3×104 parts). The combined extracts were washed with water, dried, filtered and evaporated, yielding 32 parts (100%) of N-[4-(1-hydroxy-2-methylpropyl)-2-nitrophenyl]acetamide (interm. 15).

後処理

  1. stirringUpon completion, stirring
  2. customThe reaction mixture was evaporated
  3. extractionthe residue was extracted with dichloromethane (3×104 parts)
  4. washThe combined extracts were washed with water
  5. customdried
  6. filtrationfiltered
  7. customevaporated

出典と根拠

ORDレコード
ord-2454780b224d4b35acfe35dc4a5e3dbe
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05151421

反応ノート

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