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Water → 5-Amino-[1,1'-biphenyl]-2-carboxylic acid hydrochloride

HRID 2121168
ノート
印刷プレビュー

反応式

HRID 2121168 の反応式
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[C:6]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:5]=1)([O-])=O.O.O.[Sn](Cl)[Cl:22].O.C([O-])(O)=O.[Na+]>C(OCC)(=O)C>[ClH:22].[NH2:1][C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[C:6]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:5]=1
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 962WaterHCID 61436Stannous chloride dihydrateHCID 516892Sodium BicarbonateHCID 106578414-Nitro-2-phenylbenzoic acid

生成物 1

HCID 698924925-Amino-[1,1'-biphenyl]-2-carboxylic acid hydrochloride収率 29.7%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate
溶媒

実験手順

4-Nitro-2-phenylbenzoic acid (10.5 g, 43.2 mmol) and tin(II) chloride dihydrate (34.1 g, 0.15 mol) were combined and refluxed in 250 mL ethyl acetate for 1 hour. An equal volume of water was added followed by solid NaHCO3 to pH 8. The mixture was extracted with ethyl acetate. The combined ethyl acetate extracts were washed with brine and concentrated to a thick oil. The oil was diluted with ether and excess anhydrous HCl was added. The resulting precipitate was collected and dried to provide 4-Amino-2-phenylbenzoic acid hydrochloride (3.2 g). MS m/e 214 (M+H)+. 1H NMR (d6-DMSO, 300 MHz) δ 6.65 (d, J=3 Hz, 1H), 6.79 (m, 1H), 7.20-7.72 (m, 6H).

後処理

  1. extractionThe mixture was extracted with ethyl acetate
  2. washThe combined ethyl acetate extracts were washed with brine
  3. concentrationconcentrated to a thick oil
  4. additionThe oil was diluted with ether and excess anhydrous HCl
  5. additionwas added
  6. customThe resulting precipitate was collected
  7. customdried

出典と根拠

ORDレコード
ord-aa5cfd7e2ef542c9b2da901a454c4893
出典データセット
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06693123B2

反応ノート

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