反应详情
EQUATION
反应方程式
REACTANTS
反应物
Morpholine
C4H9NO
Sodium Hydroxide
HNaO
1-Hydroxybenzotriazole
C6H5N3O
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
Methyl 5-bromo-4-methyl-2-thiophenecarboxylate
C7H7BrO2S
5-Bromo-4-methylthiophene-2-carboxylic acid
C6H5BrO2S
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
5-Bromo-4-methyl-thiophene-2-carboxylic acid methyl ester (8.51 mmol) was dissolved in EtOH (100 ml) and NaOH (42.5 mmol) added, as a 1M solution in water. Reaction was heated to 80° C. for 2 h, after which time all starting material had been consumed. Reaction was then concentrated in vacuo and the residue taken up in DCM and shaken with 1M HCl. The resulting biphasic mixture was then filtered and the filtrant washed with hexane and dried under vacuum. This gave 5-Bromo-4-methyl-thiophene-2-carboxylic acid as off white solid: m/z in MS AP−=219, 221 [M−H]−, 6.79 mmol, 80%. 5-Bromo-4-methyl-thiophene-2-carboxylic acid (6.79 mmol) was taken up in 30 ml DMF and morpholine (7.47 mmol), WSC.HCl (7.47 mmol) and HOBt (7.47 mmol) were added. Reaction was stirred at room temperature for 17 h and then diluted with EtOAc, washed with 1M HCl and brine, dried over Na2SO4 and concentrated in vacuo. Flash chromatography of the residue (silica, 33-50% EtOAc in hexane) gave (5-Bromo-4-methyl-thiophen-2-yl)-morpholin-4-yl-methanone as a pale golden oil: m/z in MS ES+=290, 292 [M+H]+, 4.67 mmol, 69%.
WORKUP
后处理
- customReaction
- customafter which time all starting material had been consumed
- customReaction
- concentrationwas then concentrated in vacuo
- filtrationThe resulting biphasic mixture was then filtered
- washthe filtrant washed with hexane
- customdried under vacuum
- customReaction
- stirringwas stirred at room temperature for 17 h
- washwashed with 1M HCl and brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo