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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Hydrochloric Acid → HCID 14404106、化合物

HRID 465502
ノート
印刷プレビュー

反応式

HRID 465502 の反応式
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10]([CH2:13][N+:14]([O-:16])=[O:15])(=[O:12])=[O:11])=[CH:6][CH:5]=1)(O)=[O:2].Cl>O1CCCC1>[OH:2][CH2:1][C:4]1[CH:9]=[CH:8][C:7]([S:10]([CH2:13][N+:14]([O-:16])=[O:15])(=[O:12])=[O:11])=[CH:6][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

4

反応物 2

HCID 313Hydrochloric AcidHCID 14404103HCID 14404103、化合物

生成物 1

HCID 14404106HCID 14404106、化合物収率 25.9%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Borane-methyl sulphide complex (0.1 ml, 1 mmol) was added to a solution of (4-carboxyphenylsulphonyl)nitromethane (0.25 g, 1 mmol) in anhydrous tetrahydrofuran (5 ml) and the mixture was stirred for 2 hours. The mixture was acidified with 2M hydrochloric acid to pH 1 and extracted with ethyl acetate. The combined extracts were dried (MgSO4) and the solvent was removed by evaporation. The residue was purified by MPLC eluting with methanol/dichloromethane (1:50 v/v) to give (4-hydroxymethylphenylsulphonyl)nitromethane (0.06 g) m.p. 73°-75° C.; microanalysis, found: C, 41.6; H, 3.9; N, 5.8%; C8H9NO5S requires: C, 41.6; H, 3.9; N, 6.1%.

後処理

  1. extractionextracted with ethyl acetate
  2. dry with materialThe combined extracts were dried (MgSO4)
  3. customthe solvent was removed by evaporation
  4. customThe residue was purified by MPLC
  5. washeluting with methanol/dichloromethane (1:50 v/v)

出典と根拠

ORDレコード
ord-75c3d65d7394459681bc7d10f53e5b14
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05153227

反応ノート

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