Hydrochloric Acid → 1-(4-Nitrophenyl)tricyclo[3.3.1.03,7]nonane-3-carboxylic acid
反応式
[OH-:1].[Na+].BrBr.Br[O-].[N+:7]([C:10]1[CH:15]=[CH:14][C:13]([C:16]23[CH2:24][CH:20]4[CH2:21][CH:22]([CH2:23]2)[C:18]([C:25](=[O:27])C)([CH2:19]4)[CH2:17]3)=[CH:12][CH:11]=1)([O-:9])=[O:8].Cl>O1CCOCC1.O>[N+:7]([C:10]1[CH:15]=[CH:14][C:13]([C:16]23[CH2:24][CH:20]4[CH2:21][CH:22]([CH2:23]2)[C:18]([C:25]([OH:1])=[O:27])([CH2:19]4)[CH2:17]3)=[CH:12][CH:11]=1)([O-:9])=[O:8]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 solution of NaOH (6.3 g, 158.0 mmol), H2O (54.0 mL) and 1,4 dioxane (7 mL) at ice bath temperature was added Br2 (3.2 mL, 59.0 mmol) and stirred for 5 minutes. The formed hypobromite solution was added dropwise to a stirred solution of 1-[1-(4-nitrophenyl)tricyclo[3.3.1.03,7]non-3-yl]ethanone (3.0 g, 10.53 mmol) obtained in step I, in 1,4-dioxane (14 mL) at ice bath temperature. The reaction mixture was gradually warmed to r.t. and after 1 h, it was cooled to ice bath temperature and acidified with conc. HCl, diluted with water, and extracted with EtOAc. The combined organic layer was washed with brine, dried over Na2SO4, and the solvent was removed under reduced pressure to obtain 1-(4-nitrophenyl)tricyclo[3.3.1.03,7]nonane-3-carboxylic acid (2.27 g) in 75% yield as off-white solid; M.R: 145-150° C. m/z (M−1) 286; IR cm−1 3437, 2945, 1693, 1596, 1511, 1408, 1352, 946, 839, 749. 1H NMR (CDCl3) 300 MHz δ 8.16 (d, J=8.8 Hz, 2H), 7.42 (d, J=8.8 Hz, 2H), 2.96-2.88 (m, 1H), 2.59-2.52 (m, 1H), 2.44-2.33 (m, 1H), 2.23-2.03 (m, 4H), 2.02-1.68 (m, 5H).
後処理
- temperatureit was cooled to ice bath temperature
- extractionextracted with EtOAc
- washThe combined organic layer was 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-1f3698823a8f469093994e8b6d7e8c2e
- 出典データセット
- uspto-grants-2011_07
- 特許番号
- US07985759B2
反応ノート
読み込み中…