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Methional → HCID 53672169, compound

HRID 581646
Notes
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Reaction equation

HRID 581646 reaction equation
Cl[CH2:2][CH2:3][CH2:4][S:5][CH3:6].[Mg].[CH3:8][S:9][CH2:10][CH2:11][CH:12]=[O:13].[Cl-].[NH4+]>C1COCC1.CCOCC>[CH3:8][S:9][CH2:10][CH2:11][CH:12]([OH:13])[CH2:2][CH2:3][CH2:4][S:5][CH3:6]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 18635MethionalHCID 25517Ammonium ChlorideHCID 5462224MagnesiumHCID 126902953-Chloropropylmethylsulfane

Product 1

HCID 53672169HCID 53672169, compoundYield 36%

Reagents, catalysts & solvents 2

HCID 3283Diethyl Ether
Solvent
HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
50 °C

Procedure

1-Chloro-3-methylthiopropane (3.73 g, 30 mmole) in dry THF (50 mL) was added to stirred magnesium turnings (0.72 g, 30 mmole) under argon. Once the addition was complete, the mixture was heated to 50° C. for 3 hours. The mixture was then allowed to cool to room temperature and 3-methylthiopropanal (3.12 g, 30 mmole) was added. The reaction was stirred at room temperature for 1 hour. 2M ammonium chloride solution (50 mL) was added, followed by ether (50 mL). The organics were separated, dried, filtered, and evaporated to give a pale yellow oil that was purified by chromatography in 40-60 petroleum ether/ether (4/5) to give 5 (2.1 g, 36%) as a colorless oil.

Workup

  1. additionOnce the addition
  2. temperatureto cool to room temperature
  3. customThe organics were separated
  4. customdried
  5. filtrationfiltered
  6. customevaporated
  7. customto give a pale yellow oil that
  8. customwas purified by chromatography in 40-60 petroleum ether/ether (4/5)

Sources & evidence

ORD record
ord-e4470f0358c64569bf7586efdb5fb652
Source dataset
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05922527

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes