反応式
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH3:11])[C:5]([OH:7])=[O:6].Cl.[N:13]([O-])=O.[Na+].C([O-])(=O)C.[Na+].[CH3:22][C:23]([SH:26])([CH3:25])[CH3:24]>O>[C:23]([S:26]/[N:13]=[N:1]/[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH3:11])[C:5]([OH:7])=[O:6])([CH3:25])([CH3:24])[CH3:22]参加物
7
反応条件
- 温度
- 0 °C
実験手順
To a mixture of 3-amino-4-methyl benzoic acid (5.0 g) in water (50 mL) was added concentrated hydrochloric acid (15 mL). The mixture was chilled to 0° C. in an ice/acetone bath. Sodium nitrite (2.28 g) was dissolved in water (10 mL) and slowly added to the mixture at 0° C. The pH was adjusted to 6 with saturated sodium acetate and 2-methyl-2-propanethiol (1.8 mL) was added. The mixture was stirred for 1 h and the resulting solids were collected by filtration, washed with water and dried under reduced pressure to give 5.7 g of the title compound: 1H NMR (CDCl3) δ 1.61, 2.20, 7.38, 7.55, 9.67.
後処理
- additionslowly added to the mixture at 0° C
- additionwas added
- filtrationthe resulting solids were collected by filtration
- washwashed with water
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-d460acee005d487d96d6209089279d3e
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07727997B2
関連ノート
読み込み中…