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4-Hydroxybenzaldehyde → 4-(3-(Diethylamino)propoxy)benzaldehyde

HRID 17651
ノート
印刷プレビュー

反応式

HRID 17651 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.C([O-])([O-])=O.[Cs+].[Cs+].S([O-])(=O)(=O)C.[CH2:21]([N:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26]O)[CH3:22].CS(Cl)(=O)=O>CS(C)=O>[CH2:21]([N:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26][O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1)[CH3:22]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 1264-HydroxybenzaldehydeHCID 10796Cesium carbonateHCID 121593-(Diethylamino)-1-propanolHCID 31297Methanesulfonyl chlorideHCID 85257Methanesulfonate

生成物 1

HCID 176070434-(3-(Diethylamino)propoxy)benzaldehyde

試薬・触媒・溶媒 1

HCID 679
Dimethyl Sulfoxide
溶媒

反応条件

温度
90 °C

実験手順

To a stirred solution of 4-hydroxybenzaldehyde (20 mmol) in DMSO (80 mL) at rt, solid Cs2CO3 (50 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride, General Procedure P2 (30 mmol) was added to the reaction mixture and heated to 90° C. until the reaction was complete. After cooling to rt, the reaction was quenched by cold H2O (100 mL), and the resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine (3×50 mL) and dried (anhydrous Na2SO4). The solvent was removed in vacuo, and the crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N) to afford 4-(3-diethylaminopropoxy)benzaldehyde.

後処理

  1. additionwas added to the reaction mixture
  2. temperatureAfter cooling to rt
  3. customthe reaction was quenched by cold H2O (100 mL)
  4. extractionthe resulting mixture was extracted with EtOAc (3×100 mL)
  5. washThe combined EtOAc extracts were washed with brine (3×50 mL)
  6. dry with materialdried (anhydrous Na2SO4)
  7. customThe solvent was removed in vacuo
  8. customthe crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N)

出典と根拠

ORDレコード
ord-db5bf796934549268433edbace0a4a79
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737285B2

反応ノート

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