反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydrochloric Acid
ClH
2 次
Dimethyl sulfate
C2H6O4S
O-Ethyl hydrogen carbonodithioate
C3H6OS2
Carbonic acid sodium salt (1:2)
CNa2O3
Sodium Hydroxide
HNaO
Disodium sulfide
Na2S
Methyl 5-amino-o-anisate
C9H11NO3
Sodium
Na
Sodium Nitrite
NNaO2
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Alternately, combine methyl 2-methoxy-5-aminobenzoate (1.0 g, 5.6 mmol) and 12 M aqueous hydrochloric acid solution (1.2 g and cool in an ice bath. Add a solution of sodium nitrite (0.37-g, 5.3 mmol) in water (3 mL). After 1.5 hours, add ethyl xanthic acid, sodium salt (0.76 g, 6.3 mmol) and sodium carbonate (0.67 g, 6.3 mmol). After 2 hours, evaporate in vacuo and add sodium sulfide (0.69 g, 2.7 mmol) and a 1 M aqueous sodium hydroxide solution (10 mL). After 4 hours, add dimethylsulfate and heat to reflux. After 24 hours, cool to ambient temperature, acidify with 12 M hydrochloric acid solution and extract with ethyl acetate. Separate the organic layer, extract with brine, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with ethyl acetate/hexane 2/1 to give methyl 2-methoxy-5-methylthiobenzoate. Elemental Analysis calculated for C9H12O3S: C, 54.53; H, 5.08. Found: C, 54.64; H, 4.95.
WORKUP
后处理
- temperaturecool in an ice bath
- waitAfter 2 hours
- customevaporate in vacuo
- waitAfter 4 hours
- temperatureheat to reflux
- waitAfter 24 hours
- extractionextract with ethyl acetate
- customSeparate the organic layer
- extractionextract with brine
- dry with materialdry over Na2SO4
- filtrationfilter
- customevaporate in vacuo
- customto give a residue