Ammonium Hydroxide → Oxane-4-carboxamide

HRID 598397Notes

Reaction equation

HRID 598397 reaction equation
[OH-].[NH4+:2].[O:3]1[CH2:8][CH2:7][CH:6]([C:9]([O:11]C)=O)[CH2:5][CH2:4]1>CO>[O:3]1[CH2:8][CH2:7][CH:6]([C:9]([NH2:2])=[O:11])[CH2:5][CH2:4]1

Participants

4

Procedure

Ammonium hydroxide (1 L) was added to a solution of methyl tetrahydro-2H-pyran-4-carboxylate (20 mL, 150 mmol) in methanol (500 mL), and the reaction was stirred overnight at ambient temperature. Additional ammonium hydroxide (500 mL) was added, and the reaction was stirred for four additional days. The methanol was removed under reduced pressure. Solid sodium chloride was added to the aqueous layer, which was extracted with chloroform (3×150 mL). The combined extracts were dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 11.4 g of tetrahydro-2H-pyran-4-carboxamide as a white solid.

Workup

  1. stirringthe reaction was stirred for four additional days
  2. customThe methanol was removed under reduced pressure
  3. additionSolid sodium chloride was added to the aqueous layer, which
  4. extractionwas extracted with chloroform (3×150 mL)
  5. dry with materialThe combined extracts were dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-602a3901f5b3499d950d4ed1c786ac64
Source dataset
uspto-grants-2011_03
Patent number
US07897597B2

Reaction notes

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