反応式
[CH:1]1[C:9](=[N:10]O)[CH:8]=[CH:7][C:5](=[O:6])[C:3](=[O:4])[CH:2]=1.[Sn](Cl)Cl>C(O)C>[CH:1]1[C:9]([NH2:10])=[CH:8][CH:7]=[C:5]([OH:6])[C:3](=[O:4])[CH:2]=1参加物
4
実験手順
To a stirred solution of 0.39 g of 5-nitrosotropolone (2.6 mmole, obtained from the previous example) and 10 mL of absolute ethanol was added 2.92 g of Tin (II) chloride (12.9 mmole). After 40 minutes at reflux the solution was cooled, filtered, and the liquefied portion was partitioned between ethyl acetate and water. The organic fraction was concentrated in vacuo to give 35 mg (10%) of 5-aminotropolone as a yellow solid. IR spectroscopy of the product (neat) found the following characteristic IR absorption frequencies: 3319 cm−1, 3181 cm−1, 2925 cm−1, 1511 cm−1, 1410 cm−1, 1261 cm−1, 837 cm−1, 781 cm−1, and 739 cm−1.
後処理
- temperatureAfter 40 minutes at reflux the solution
- temperaturewas cooled
- filtrationfiltered
- customthe liquefied portion was partitioned between ethyl acetate and water
- concentrationThe organic fraction was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-19d79bc842754776ae91909a491a169b
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07867774B2
関連ノート
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