反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
16.2 g of (-)-S-Methyl-L-cysteine (0.1 mol) are suspended in a mixture of 120 ml of water and 120 ml of acetone in a four-necked flask under N2. 30.4 ml (22.2 g) of triethylamine (0.22 mol) are added rapidly while stirring. 15.9 g of 2,4-difluoronitrobenzene (0.1 mol) are added, with further stirring, to the resulting yellow solution. The mixture is heated to reflux for 7.5 hours while stirring (orange-colored solution) and the acetone is then stripped off under reduced pressure on a rotary evaporator; the aqueous residue is transferred to a separating funnel and extracted 2× with approximately 50 ml of methyl tert-butyl ether (MTB ether). This extract is composed, in the main, of 2,4-difluoronitrobenzene and is discarded. The aqueous phase is transferred to a four-necked flask and 150 ml of MTB ether are added to it, after which the mixture is adjusted, while being cooled (<25° C.), to pH 1 with approximately 25 ml of 38% sulfuric acid. The mixture is then stirred thoroughly until clear phases are formed. The ether phase is separated off and the aqueous phase is extracted once again with 50 ml of MTB ether. The extracts are dried over sodium sulfate and evaporated on a rotary evaporator. The yield comprises 27 g of a yellow oil which soon solidifies. M.p. 147° (from water/methanol).
WORKUP
后处理
- temperatureThe mixture is heated
- temperatureto reflux for 7.5 hours
- stirringwhile stirring (orange-colored solution)
- customthe acetone is then stripped off under reduced pressure on a rotary evaporator
- customthe aqueous residue is transferred to a separating funnel
- extractionextracted 2× with approximately 50 ml of methyl tert-butyl ether (MTB ether)
- customThe aqueous phase is transferred to a four-necked flask
- addition150 ml of MTB ether are added to it
- temperaturewhile being cooled (<25° C.)
- stirringThe mixture is then stirred thoroughly until clear phases
- customare formed
- customThe ether phase is separated off
- extractionthe aqueous phase is extracted once again with 50 ml of MTB ether
- dry with materialThe extracts are dried over sodium sulfate
- customevaporated on a rotary evaporator