2H-Pyran-4-carboxylic acid, tetrahydro-, methyl ester → Oxane-4-carboxamide
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([C:7]([O:9]C)=O)[CH2:3][CH2:2]1.O.[NH3:12]>>[O:1]1[CH2:6][CH2:5][CH:4]([C:7]([NH2:12])=[O:9])[CH2:3][CH2:2]1Participants
3
Procedure
To methyl tetrahydro-2H-pyran-4-carboxylate (50 g, 347 mmol) was added concentrated ammonia water (50 mL), and the reaction mixture was stirred at room temperature for 43.5 hours. Thereafter, the reaction mixture was cooled in an ice water bath, and the precipitate was filtrated. Then, the precipitate was dried at 40° C. under reduced pressure, to obtain 33.4 g of a title compound (yield: 74.6%).
Workup
- temperatureThereafter, the reaction mixture was cooled in an ice water bath
- filtrationthe precipitate was filtrated
- customThen, the precipitate was dried at 40° C. under reduced pressure
Sources & evidence
- ORD record
- ord-52cee181ad674e5d8c576a9baf01d46a
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858809B2
Reaction notes
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