Sodium Hydroxide → HCID 22244582, compound

HRID 891073Notes

Reaction equation

HRID 891073 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][OH:10])=[CH:4][CH:3]=1.[N+:11]([O-])([O-])=O.[Na+].O.O.[Sn](Cl)Cl.[C:21]([CH2:24][C:25](=O)[CH3:26])(=O)[CH3:22].[OH-].[Na+]>Cl.O>[CH3:22][C:21]1[CH:24]=[C:25]([CH3:26])[N:1]([C:2]2[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][OH:10])=[CH:4][CH:3]=2)[N:11]=1

Participants

8

Procedure

To a suspension of 4-aminophenylethylalcohol (7.27 g, 51.5 mmol) in conc. HCl (100 mL) was added dropwise a solution of sodium nitrate (3.9 g, 56 mmol) in water (100 mL) at −10° C. over 0.5 h. After stirring for 0.5 h, tin(II) chloride dihydrate (29 g, 128 mmol) in conc.HCl (100 mL) was added over 0.5 h and the resulting mixture was allowed to warm to room temperature. The mixture was stirred for 1 h and then added acetylacetone. The reaction mixture was warmed at 100° C. for 5 h. It was basified with aqueous NaOH (pH˜10). The mixture was extracted with dichloromethane, dried (Na2SO4), and evaporated to give the title compound quantitatively: MS (ESI) m/z 217 [M+H]+, 1H-NMR (CDCl3) δ 7.34-7.24 (4H, m), 5.98 (1H, s), 3.73 (2H, m), 2.84 (2H, m), 2.28 (3H, s), 2.27 (s, 3H).

Workup

  1. stirringThe mixture was stirred for 1 h
  2. temperatureThe reaction mixture was warmed at 100° C. for 5 h
  3. extractionThe mixture was extracted with dichloromethane
  4. dry with materialdried (Na2SO4)
  5. customevaporated

Sources & evidence

ORD record
ord-c0e3327a0be3448c94cafc2f0fd66849
Source dataset
uspto-grants-2006_02
Patent number
US07001917B2

Reaction notes

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