反応 #1339726

ord-261addd97fb74149b1d3364fb006f437

反応方程式

COc1c(C)c(C)c(OC)c(C=O)c1C
2,5-dimethoxy-3,4,6-trimethylbenzaldehyde
CC(=O)C(=O)[O-].[Na+]
sodium pyruvate
[K+].[OH-]
potassium hydroxide
COc1c(C)c(C)c(OC)c(C=CC(=O)C(=O)O)c1C
4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid
収率 100.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the mixture is subsequently heated
  2. 2
    温度at reflux for 5 hours
  3. 3
    その他whereby a yellow solution is obtained
  4. 4
    その他the resulting 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid is precipitated by the addition of sulphuric acid
  5. 5
    workup.STIRRINGThe suspension is stirred for 1 hour
  6. 6
    ろ過filtered
  7. 7
    洗浄the filter residue is washed with water
  8. 8
    その他dried

実験手順

A suspension of 3.7 g (17.6 mmol) of 2,5-dimethoxy-3,4,6-trimethylbenzaldehyde and 5.0 g (53.2 mmol) of sodium pyruvate in 20 ml of methanol is treated with 0.1 g (1.8 mmol) of potassium hydroxide and the mixture is subsequently heated at reflux for 5 hours, whereby a yellow solution is obtained. The reaction mixture is poured on to ice-water and the resulting 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid is precipitated by the addition of sulphuric acid while stirring. The suspension is stirred for 1 hour, filtered, the filter residue is washed with water and dried. In this manner there are obtained 4.9 g of 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid in the form of a yellow powder of melting point 126°-127° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04743696uspto-grants-1988_05