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Sodium sulfate decahydrate → 1-{5-Chloro-2-[(1-methylethyl)sulfanyl]phenyl)methanamine hydrochloride

HRID 1015741
Notes
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Reaction equation

HRID 1015741 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([S:16][CH:17]([CH3:19])[CH3:18])=[C:12]([CH:15]=1)[C:13]#[N:14].O.O.O.O.O.O.O.O.O.O.[O-]S([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[ClH:7].[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([S:16][CH:17]([CH3:19])[CH3:18])=[C:12]([CH2:13][NH2:14])[CH:15]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 62649Sodium sulfate decahydrateHCID 21226445Aluminium lithium hydrideHCID 624939095-Chloro-2-[(1-methylethyl)sulfanyl]benzonitrile

Product 1

HCID 668785341-{5-Chloro-2-[(1-methylethyl)sulfanyl]phenyl)methanamine hydrochlorideYield 152.1%

Reagents, catalysts & solvents 1

HCID 8028Tetrahydrofuran
Solvent
2×

Procedure

(Step 2) To a suspension of lithium aluminum hydride (1.56 g) in tetrahydrofuran (250 ml) was added a solution of 5-chloro-2-[(1-methylethyl)sulfanyl]benzonitrile obtained in Step 1 (7.25 g) in tetrahydrofuran (50 ml) at 0° C. The mixture was stirred at room temperature for 3 hr, and treated with sodium sulfate 10 hydrate. The mixture was further stirred at room temperature for 30 min, and the inorganic substance was filtered off through celite. The filtrate was concentrated under reduced pressure. The residue was dissolved in methanol, 4N hydrogen chloride-ethyl acetate solution (15 ml) was added, and the solvent was evaporated under reduced pressure. The obtained solid was washed with a mixed solvent of diisopropyl ether-ethyl acetate to give 1-{5-chloro-2-[(1-methylethyl)sulfanyl]phenyl}methanamine hydrochloride (6.57 g).

Workup

  1. stirringThe mixture was further stirred at room temperature for 30 min
  2. filtrationthe inorganic substance was filtered off through celite
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in methanol
  5. addition4N hydrogen chloride-ethyl acetate solution (15 ml) was added
  6. customthe solvent was evaporated under reduced pressure
  7. washThe obtained solid was washed with a mixed solvent of diisopropyl ether-ethyl acetate

Sources & evidence

ORD record
ord-e3aa450a32e940d4a4a1443b2285f16d
Source dataset
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07985862B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes