反応式
[CH2:1]1[C:6]2([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]2)[CH2:5][CH2:4][NH:3][CH2:2]1.[C:12](OC(=O)C)(=[O:14])[CH3:13]>O1CCCC1>[C:12]([N:3]1[CH2:4][CH2:5][C:6]2([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]2)[CH2:1][CH2:2]1)(=[O:14])[CH3:13]参加物
4
実験手順
A solution of 7 ml of 3-azaspiro[5.5]undecane and 9.7 ml of acetic anhydride in 19.5 ml of tetrahydrofuran was refluxed for 3 hours. The volatiles were evaporated to a yellow oil which was distilled in a Kugelrohr still giving a yellow oil, BP 90°-100° C./200-atm. The distillate was purified by chromatography on silica gel using 1:1 ethyl acetate:hexanes giving 7.89 g of the desired product as a colorless oil.
後処理
- customThe volatiles were evaporated to a yellow oil which
- distillationwas distilled in a Kugelrohr
- customstill giving a yellow oil, BP 90°-100° C./200-atm
- distillationThe distillate was purified by chromatography on silica gel using 1:1 ethyl acetate
出典と根拠
- ORDレコード
- ord-d318633b5f464a62b74f0062febe4b8e
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04965284
関連ノート
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