Sodium sulfate decahydrate → 4-Amino-3,5-dichlorobenzylamine

HRID 1819674Notes

Reaction equation

HRID 1819674 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:7][C:8]1[CH:9]=[C:10]([CH:13]=[C:14]([Cl:17])[C:15]=1[NH2:16])[C:11]#[N:12].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+]>C1COCC1>[Cl:7][C:8]1[CH:9]=[C:10]([CH:13]=[C:14]([Cl:17])[C:15]=1[NH2:16])[CH2:11][NH2:12]

Participants

5

Reactant 3

HCID 62649Sodium sulfate decahydrateHCID 5227064-Amino-3,5-dichlorobenzonitrileHCID 21226445Aluminium lithium hydride

Product 1

HCID 189757634-Amino-3,5-dichlorobenzylamine

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

Step A (1): To lithium aluminum hydride (0.57 g, 15 mmol) in dry THF (20 mL) was added dropwise 3,5-dichloro-4-aminobenzonitrile (1.87 g, 10 mmol) in THF (30 mL). The mixture was stirred at rt for 2 h. Then, sodium sulfate decahydrate (4.83 g, 15 mmol) was added and the mixture was stirred for 30 min. The solid was filtered off and washed with THF three times. The solvent was removed under vacuum and the residue was purified by chromatography with Methanol/DCM (3:7) as the eluant. 3,5-Dichloro-4-aminobenzylamine was obtained as an off-white solid (1.5 g, 80%). 1H NMR (300 MHz, CD3OD): δ3.65 (s, 2H), 7.2 (s, 2H).

Workup

  1. stirringthe mixture was stirred for 30 min
  2. filtrationThe solid was filtered off
  3. washwashed with THF three times
  4. customThe solvent was removed under vacuum
  5. customthe residue was purified by chromatography with Methanol/DCM (3:7) as the eluant

Sources & evidence

ORD record
ord-fcdee6e78fbb4a09b1ef1edc2fd5eb5a
Source dataset
uspto-grants-2009_10
Patent number
US07601751B2

Reaction notes

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