3-(Diethylamino)phenol → 3-[(3-bromopropyl)oxy]-N,N-diethylaniline

HRID 1724967ノート

反応式

HRID 1724967 の反応式
[CH2:1]([N:3]([CH2:11][CH3:12])[C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1)[CH3:2].[Br:13][CH2:14][CH2:15][CH2:16]Br.C([O-])([O-])=O.[Cs+].[Cs+]>C(#N)C>[Br:13][CH2:14][CH2:15][CH2:16][O:10][C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=1)[N:3]([CH2:1][CH3:2])[CH2:11][CH3:12]

参加物

5

反応物 3

HCID 70623-(Diethylamino)phenolHCID 80011,3-DibromopropaneHCID 10796Cesium carbonate

生成物 1

HCID 689633743-[(3-bromopropyl)oxy]-N,N-diethylaniline収率 17.4%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a solution of 3-(diethylamino)phenol (0.0104 g, 0.631 mmol) in acetonitrile (4 mL) was added 1,3-dibromopropane (0.640 mL, 6.30 mmol) followed by Cs2CO3 (0.313 g, 0.961 mmol). The reaction mixture was stirred for 24 h and then concentrated under vacuum. The resulting residue was treated with H2O (4 mL) and extracted with DCM (8 mL). The organic layer was dried through a phase separator and concentrated under vacuum. The residue was taken up in DMSO and purified by preparatory HPLC (without TFA) to give the title compound (0.0314 g, 17.4%). EI-MS m/z 286(M+H+) Rt (1.59 min).

後処理

  1. concentrationconcentrated under vacuum
  2. additionThe resulting residue was treated with H2O (4 mL)
  3. extractionextracted with DCM (8 mL)
  4. customThe organic layer was dried through a phase separator
  5. concentrationconcentrated under vacuum
  6. custompurified by preparatory HPLC (without TFA)

出典と根拠

ORDレコード
ord-c1e4bb39676343a7be38d4edf755c36b
出典データセット
uspto-grants-2009_02
特許番号
US07488827B2

反応ノート

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