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Sodium Hydroxide → HCID 17952314、化合物

HRID 456480
ノート
印刷プレビュー

反応式

HRID 456480 の反応式
C[O:2][C:3](=[O:17])[CH2:4][CH:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][N:6]1[CH:14]([CH3:16])[CH3:15].[OH-].[Na+]>CO>[CH:14]([N:6]1[CH2:7][C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]1[CH2:4][C:3]([OH:17])=[O:2])([CH3:16])[CH3:15]
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 14798Sodium HydroxideHCID 69219063(2-isopropyl-2,3-dihydro-1H-isoindol-1-yl)-acetic acid methyl ester

生成物 1

HCID 17952314HCID 17952314、化合物収率 85.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To the compound of Step B (0.53 g., 2.30 mmol) in MeOH (5.1 mL) was added 1.0N NaOH (2.53 mL, 2.53 mmol). After two days, the solution was concentrated to dryness. The resulting residue was diluted with 1.0N HCl and water was loaded onto a strong cation exchange resin. The resin was washed with water, THF/water (1:1) and then water. The product was then eluted from the resin with pyridine/water (1:9). The eluent was concentrated to dryness to afford about 0.43 g (85%) of the final compound. EIS-MS 220 [M+1].

後処理

  1. concentrationthe solution was concentrated to dryness
  2. additionThe resulting residue was diluted with 1.0N HCl and water
  3. washThe resin was washed with water, THF/water (1:1)
  4. washThe product was then eluted from the resin with pyridine/water (1:9)
  5. concentrationThe eluent was concentrated to dryness

出典と根拠

ORDレコード
ord-fd6fc22594dd43b5b40298bed920acba
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07186715B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート