Sodium Sulfate → HCID 178470904, compound

HRID 1467557Notes

Reaction equation

HRID 1467557 reaction equation
[CH2:1]([O:3][CH:4]([O:13][CH2:14][CH3:15])[C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH:8]=O)[CH3:2].S([O-])([O-])(=O)=O.[Na+].[Na+].[NH2:23][C:24]1[CH:32]=[CH:31][CH:30]=[C:29]2[C:25]=1[CH2:26][O:27][C:28]2=[O:33]>ClCCl>[CH2:1]([O:3][CH:4]([O:13][CH2:14][CH3:15])[C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)/[CH:8]=[N:23]/[C:24]1[CH:32]=[CH:31][CH:30]=[C:29]2[C:25]=1[CH2:26][O:27][C:28]2=[O:33])[CH3:2]

Participants

5

Reactant 3

HCID 24436Sodium SulfateHCID 122846494-Amino-1,3-dihydro-2-benzofuran-1-oneHCID 162177103-(Diethoxymethyl)benzaldehyde

Product 1

HCID 178470904HCID 178470904, compoundYield 61%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a stirred mixture of 3-(diethoxymethyl)benzaldehyde (3.75 g, 18 mmol) and anhydrous sodium sulfate (21.3 g, 150 mmol) in anhydrous dichloromethane (300 mL) was added 4-aminoisobenzofuran-1(3H)-one (2.24 g, 15 mmol) at 0° C. After the addition, the mixture was stirred at room temperature for 6 days. The mixture was filtered and the cake was washed with dichloromethane (50 mL×3). The filtrate was concentrated to give crude product. The crude product was washed with petroleum ether to give (E)-4-(3-(diethoxymethyl)benzylideneamino)isobenzofuran-1(3H)-one (3.1 g, yield 61%) as a white solid. LC-MS (ESI) m/z: 340 (M+1)+.

Workup

  1. additionAfter the addition
  2. filtrationThe mixture was filtered
  3. washthe cake was washed with dichloromethane (50 mL×3)
  4. concentrationThe filtrate was concentrated
  5. customto give crude product
  6. washThe crude product was washed with petroleum ether

Sources & evidence

ORD record
ord-b04cd6c13e454fc78933498d3e429e7b
Source dataset
uspto-grants-2015_04
Patent number
US08999987B2

Reaction notes

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