Hydrochloric Acid → 1-(4-Nitrophenyl)tricyclo[3.3.1.03,7]nonane-3-carboxylic acid

HRID 1015516ノート

反応式

HRID 1015516 の反応式
[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

8

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

  1. temperatureit was cooled to ice bath temperature
  2. extractionextracted with EtOAc
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. 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

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