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Methanol → 2-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dihyrothiophene

HRID 1949133
Notes
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Reaction equation

HRID 1949133 reaction equation
CO.[NH2-].[Na+].[Cl:5][C:6]1[CH:7]=[C:8]([CH:13]([S:18][CH2:19][CH2:20][C:21](=[O:23])[CH3:22])[C:14]([O:16]C)=O)[CH:9]=[CH:10][C:11]=1[Cl:12].[Cl-].[NH4+]>O>[Cl:5][C:6]1[CH:7]=[C:8]([CH:13]2[C:14]([OH:16])=[C:20]([C:21]([CH3:22])=[O:23])[CH2:19][S:18]2)[CH:9]=[CH:10][C:11]=1[Cl:12]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 887Methanol2×HCID 24533Sodium amideHCID 25517Ammonium ChlorideHCID 58281519Methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate

Product 1

HCID 442070402-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dihyrothiopheneYield 69.3%

Reagents, catalysts & solvents 1

HCID 962
Water
Solvent

Conditions

Temperature
40 °C

Procedure

A methanol (500 mL) solution of sodium amide (19.2 g, purity: 90%, 1.5 equivalent amounts based on the starting material) was heated to 40° C., and to this solution, a methanol (200 mL) solution of methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate (100 g, purity: 95%, 296 mmol) was dropwise added over a period of 12 minutes, followed by stirring at 40° C. for 1 hour. The reaction solution was cooled to 5° C., water (300 mL) was dropwise added over a period of 10 minutes, and then the solvent was distilled off. To the obtained crude product, chloroform and a saturated ammonium chloride aqueous solution were added, followed by liquid separation, and the organic layer was washed with a saturated salt solution and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off to give the desired product as an oil (59.3 g, yield: 65%).

Workup

  1. temperatureThe reaction solution was cooled to 5° C.
  2. distillationthe solvent was distilled off
  3. customTo the obtained crude product, chloroform
  4. customfollowed by liquid separation
  5. washthe organic layer was washed with a saturated salt solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe drying agent was removed by filtration
  8. distillationthe solvent was distilled off

Sources & evidence

ORD record
ord-ab7b960c34b94f909af9147d38110052
Source dataset
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08399685B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes