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Acetic Acid → HCID 14990620、化合物

HRID 2166042
ノート
印刷プレビュー

反応式

HRID 2166042 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[O:9])=[CH:4][C:3]=1[N+:16]([O-:18])=[O:17].CO.[BH4-].[Na+].C(O)(=O)C>O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[OH:9])=[CH:4][C:3]=1[N+:16]([O-:18])=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 176Acetic AcidHCID 887MethanolHCID 4311764Sodium borohydrideHCID 14590583(4-Fluoro-3-nitrophenyl)(phenyl)methanone

生成物 1

HCID 14990620HCID 14990620、化合物収率 100%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a cooled (ice bath) solution of 24.5 parts of (4-fluoro-3-nitrophenyl) phenylmethanone in 120 parts of methanol were added portionwise 1.5 parts of sodium tetrahydroborate. Upon complete addition, stirring was continued for 15 minutes at 0° C. A solution of 3 parts of acetic acid in 25 parts of water was added dropwise to the mixture. Upon completion, the mixture was concentrated. Water was added to the residue and the product was extracted with dichloromethane. The extract was dried, filtered and concentrated, yielding 25.1 parts (100%) of 4-fluoro-3-nitro-α-phenylbenzenemethanol as an oily residue (int. 63).

後処理

  1. additionUpon complete addition
  2. concentrationUpon completion, the mixture was concentrated
  3. additionWater was added to the residue
  4. extractionthe product was extracted with dichloromethane
  5. customThe extract was dried
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-e7a3f7a9422c4786b95b933d29958c6e
出典データセット
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04943574

反応ノート

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