反応式
[O:1]1[CH2:6][CH2:5][CH:4]([C:7]([O:9]C)=O)[CH2:3][CH2:2]1.[NH3:11]>>[O:1]1[CH2:6][CH2:5][CH:4]([C:7]([NH2:11])=[O:9])[CH2:3][CH2:2]1参加物
3
実験手順
Concentrated aqueous ammonia (50 mL) was added to methyl tetrahydro-2H-pyran-4-carboxylate (50 g, 347 mmol) and the reaction mixture was stirred for 43.5 hours at room temperature. The reaction mixture was then cooled in an ice water bath, after which the precipitate was filtered out and dried under reduced pressure at 40° C. to afford 33.4 g of the title compound (74.6% yield).
後処理
- temperatureThe reaction mixture was then cooled in an ice water bath
- filtrationafter which the precipitate was filtered out
- customdried under reduced pressure at 40° C.
出典と根拠
- ORDレコード
- ord-252e002dbf1d499fbd2f04606d198237
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07176216B2
関連ノート
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