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