反応式
[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([CH:16]=[C:17]2[S:21][CH2:20][N:19]([CH2:22][CH2:23][O:24]C(=O)C)[C:18]2=[O:28])[CH:8]=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:10]=1[OH:11])([CH3:4])[CH3:3].[OH-].[NH4+]>C(#N)C>[CH3:15][C:12]([C:9]1[CH:8]=[C:7]([CH:16]=[C:17]2[S:21][CH2:20][N:19]([CH2:22][CH2:23][OH:24])[C:18]2=[O:28])[CH:6]=[C:5]([C:2]([CH3:1])([CH3:3])[CH3:4])[C:10]=1[OH:11])([CH3:13])[CH3:14]参加物
実験手順
A solution of 85.2 g of 5-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-[2-(acetyloxy)ethyl]-4-thiazolidinone from Example 26 in 1.5 l of acetonitrile was treated with 1 1 of concentrated ammonium hydroxide. The reaction mixture was allowed to stand for approximately 90 hours at room temperature. The solution was concentrated in vacuo and 500 ml of ethyl acetate were added, with the pH adjusted to 3.0 with concentrated hydrochloric acid. The layers were separated and the aqueous layer extracted with 250 ml of ethyl acetate. The combined organic layers were washed with 250 ml of a saturated sodium chloride solution and concentrated in vacuo. The residue was crystallized from 95 ml of hexane and 70 ml of ethyl acetate to provide 35.68 g of the desired subtitled intermediate, m.p. 131-135° C.
後処理
- concentrationThe solution was concentrated in vacuo and 500 ml of ethyl acetate
- additionwere added, with the pH
- customThe layers were separated
- extractionthe aqueous layer extracted with 250 ml of ethyl acetate
- washThe combined organic layers were washed with 250 ml of a saturated sodium chloride solution
- concentrationconcentrated in vacuo
- customThe residue was crystallized from 95 ml of hexane and 70 ml of ethyl acetate
出典と根拠
- ORDレコード
- ord-b1ff61e2676f4293b5c491746c18cf7d
- 出典データセット
- uspto-grants-1992_10
- 特許番号
- US05158966
関連ノート
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