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Formic Acid → 4-(4-Chloro-butoxy)-2-(naphthalene-1-sulfonylmethyl)-phenyl amine

HRID 2240043
ノート
印刷プレビュー

反応式

HRID 2240043 の反応式
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([N+:27]([O-])=O)=[C:11]([CH2:13][S:14]([C:17]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:20]=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH:12]=1.C(O)=O>C1COCC1.CO.[Pd]>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([NH2:27])=[C:11]([CH2:13][S:14]([C:17]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:20]=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH:12]=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 2

HCID 284Formic AcidHCID 686789021-[5-(4-Chloro-butoxy)-2-nitro-phenylmethanesulfonyl]-naphthalene

生成物 1

HCID 686794554-(4-Chloro-butoxy)-2-(naphthalene-1-sulfonylmethyl)-phenyl amine収率 84.4%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 887Methanol溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

A mixture of 1-[5-(4-chloro-butoxy)-2-nitro-phenyl-methanesulfonyl]-naphthalene (1.94 g, 4.5 mmoles) and 10% Pd/C in THF (20 mL), methanol (20 mL), and formic acid (5 mL) was hydrogenated in a Parr hydrogenation bottle (250 mL) at 40 lb/in2 for 20 hours. The mixture was filtered through Celite, and the filtrate was diluted with EtOAc, washed with water, dried over Na2SO4, and concentrated under vacuum. The crude product was purified by flash chromatography using as eluent 5% EtOAc/CH2Cl2 to afford the title compound as an off-white solid (1.54 g, 3.8 mmoles).

後処理

  1. filtrationThe mixture was filtered through Celite
  2. additionthe filtrate was diluted with EtOAc
  3. washwashed with water
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under vacuum
  6. customThe crude product was purified by flash chromatography

出典と根拠

ORDレコード
ord-375bc30268a64b20b6a37d0af190b9f4
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723329B2

反応ノート

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