Acetic Acid → 1-(2-Oxopyrrolidin-1-yl)tricyclo[3.3.1.03,7]nonane-3-carboxylic acid
反応式
[OH-].[Na+].BrBr.Br[O-].[C:7]([C:10]12[CH2:17][CH:16]3[CH2:18][C:12]([N:19]4[CH2:23][CH2:22][CH2:21][C:20]4=[O:24])([CH2:13][CH:14]1[CH2:15]3)[CH2:11]2)(=[O:9])C.C(O)(=[O:27])C>O1CCOCC1.O>[O:24]=[C:20]1[CH2:21][CH2:22][CH2:23][N:19]1[C:12]12[CH2:18][CH:16]3[CH2:15][CH:14]([CH2:13]1)[C:10]([C:7]([OH:9])=[O:27])([CH2:17]3)[CH2:11]2参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a stirred mixture of NaOH (2.4 g, 60.6 mmol), H2O (16 mL) and 1,4 dioxane (4 mL) at ice bath temperature was added Br2 (1.13 mL, 22.6 mmol) and stirred for 5 minutes. The resulting hypobromite solution was added dropwise to a stirred solution of the compound obtained in step I (1.0 g, 4.04 mmol) in 1,4-dioxane (18 mL) at 10° C. The temperature of the reaction was brought to room temperature and the reaction mixture was stirred for 1 h. Then it was cooled to ice bath temperature and quenched by adding acetic acid (3.9 mL, 65.7 mmol). The reaction mixture was diluted with water, extracted with EtOAc, and the combined organic layers were washed with brine and dried over Na2SO4. The solvent was removed under reduced pressure to obtain 1-(2-oxopyrrolidin-1-yl)tricyclo[3.3.1.03,7]nonane-3-carboxylic acid as a viscous liquid (1.3 g) in 100% yield. m/z (M+1) 250; 1H NMR (CDCl3) 300 MHz δ 3.42 (t, J=7.0 Hz, 2H), 2.78-2.71 (m, 1H), 2.47-2.23 (m, 6H), 2.08-1.90 (m, 6H), 1.85-1.72 (m, 2H), 1.62 (dd, J=2.4, 11.0 Hz, 1H).
後処理
- customwas brought to room temperature
- stirringthe reaction mixture was stirred for 1 h
- temperatureThen it was cooled to ice bath temperature
- customquenched
- extractionextracted with EtOAc
- washthe combined organic layers were washed with brine
- dry with materialdried over Na2SO4
- customThe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-b5c0471d00c94f29abb142149b274e5d
- 出典データセット
- uspto-grants-2011_07
- 特許番号
- US07985759B2
反応ノート
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