反応 #4491

ord-7c9f173d9c7d4c9db041ee6af88f9112

反応方程式

CC(=O)O
acetic acid
[BH4-].[Na+]
Sodium borohydride
Cc1nc(C(=O)COc2ccc(C=C3SC(=O)NC3=O)cc2)c(C)o1
5-{4-[2-(2,5-dimethyl-oxazolyl)-2-oxoethoxy]benzylidene}-2,4-thiazolidinedione
Cc1nc(C(O)COc2ccc(CC3SC(=O)NC3=O)cc2)c(C)o1
5-{4-[2-(2,5-dimethyl-4-oxazolyl)-2-hydroxyethoxy]benzyl}-2,4-thiazolidinedione
収率 97.5%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooling
  2. 2
    温度cooling for 20 minutes
  3. 3
    その他the crystals which separated out
  4. 4
    ろ過were collected by filtration

実験手順

Sodium borohydride (0.16 g) was added to a suspension of 5-{4-[2-(2,5-dimethyl-oxazolyl)-2-oxoethoxy]benzylidene}-2,4-thiazolidinedione (1.5 g) in methanol-N,N-dimethylformamide (1:1, V.V, 40 ml) under ice-cooling. After stirring under ice-cooling for 20 minutes, the reaction solution was poured into ice-water, and the aqueous mixture was made acid with acetic acid, and the crystals which separated out were collected by filtration to give 5-{4-[2-(2,5-dimethyl-4-oxazolyl)-2-hydroxyethoxy]benzyl}-2,4-thiazolidinedione (1.47 g, 97.5%). Recrystallization from chloroform-ethanol afforded colorless prisms, m.p. 223°-224° C. Elemental analysis for C17H16N2O5S, Calcd.: C, 56.66; H, 4.47; N, 7.77. Found: C, 56.36; H, 4.55; N, 7.56.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04725610uspto-grants-1988_02