反応 #1613

ord-275e8400c15942e28e2a52018fda7f14

反応方程式

COc1ccc(C(=O)[O-])c(C)c1[N+](=O)[O-]
3-nitro-4-methoxy-methylbenzoate
[K+].[OH-]
potassium hydroxide
COc1ccc(C(=O)O)cc1[N+](=O)[O-]
product
収率 76.6%
COc1ccc(C(=O)O)cc1[N+](=O)[O-]
3-nitro-4-methoxy benzoic acid
収率 76.6%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過after which the resulting solid was collected by vacuum filtration
  2. 2
    洗浄washed with 2×100 ml of ethyl ether
  3. 3
    workup.DISSOLUTIONThe solid was dissolved in 200 ml of water
  4. 4
    ろ過The resulting precipitate was collected by vacuum filtration
  5. 5
    洗浄washed with 200 ml water
  6. 6
    その他dried overnight in vacuo at 30° C

実験手順

To a 500 ml erlenmeyer flask with magnetic stirrer was charged 10.3 g of 3-nitro-4-methoxy-methylbenzoate, 400 ml tetrahydrofuran, and 3.2 g of 86% potassium hydroxide. The reaction was stirred for 12 hours at ambient temperature, after which the resulting solid was collected by vacuum filtration and washed with 2×100 ml of ethyl ether. The solid was dissolved in 200 ml of water and acidified to pH 4 with 6N hydrochloric acid. The resulting precipitate was collected by vacuum filtration, washed with 200 ml water, and dried overnight in vacuo at 30° C. Isolated 7.4 g of product as a white solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726162uspto-grants-1998_03