Methanol → Methyl 3-oxotetrahydrothiopyran-2-carboxylate

HRID 656027Notes

Reaction equation

HRID 656027 reaction equation
[Na].CO.[CH3:4][O:5][C:6](=[O:16])[CH2:7][S:8][CH2:9][CH2:10][CH2:11][C:12](OC)=[O:13]>C1(C)C=CC=CC=1>[O:13]=[C:12]1[CH2:11][CH2:10][CH2:9][S:8][CH:7]1[C:6]([O:5][CH3:4])=[O:16]

Participants

5

Procedure

To a suspension of sodium (3.5 g, 0.15 mol) in dry toluene (300 mL) was added an excess of methanol (30 mL). After sodium was disappeared, the excess methanol was removed as the methanol-toluene azeotrope. When the distillation temperature had reached 105° C., Methyl 4-{[2-(methyloxy)-2-oxoethyl]thio}butanoate (28.3 g, 0.14 mol) in toluene (90 mL) was added over a period of ten mins. The methanol-toluene azeotrope was removed by distillation, after the distillation temperature rose to 106° C., the reaction mixture was cooled to room temperature. The reaction mixture was poured into a mixture of ice (100 g) and 12N HCl (20 mL). The organic layer was removed and the aqueous layer was extracted with three 60 mL portions of ether and the combined organic layers were dried over Na2SO4. After removing the solvent, 23.4 g of crude product was obtained (Yield: 96%).

Workup

  1. customthe excess methanol was removed as the methanol-toluene azeotrope
  2. customhad reached 105° C.
  3. customThe methanol-toluene azeotrope was removed by distillation
  4. customrose to 106° C.
  5. additionThe reaction mixture was poured into a mixture of ice (100 g) and 12N HCl (20 mL)
  6. customThe organic layer was removed
  7. extractionthe aqueous layer was extracted with three 60 mL portions of ether
  8. dry with materialthe combined organic layers were dried over Na2SO4
  9. customAfter removing the solvent

Sources & evidence

ORD record
ord-b539efb6b4e648cbb53db45eb3680496
Source dataset
uspto-grants-2011_12
Patent number
US08071584B2

Reaction notes

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