Chlorotrimethylsilane → N-(4-carboxybenzyl)hexanamide

温度

-20 °C

Hexanoic acid (3.06 g) in 20 mL acetonitrile is treated with N-methylmorpholine (2.9 mL) and the mixture cooled to -20° C. with stirring. Ethyl chloroformate (2.8 mL) is then added dropwise, keeping the temperature below or at -20° C. After stirring for an additional 40 min at that temperature, the solution is transferred to a cooled (-15° C.) solution of alphaamino-p-toluic acid (2.0 g), triethylamine (15 mL), a chlorotrimethylsilane (5.0 mL) in methylene chloride (60 mL; prepared as described in Example 7). After the addition is complete, the mixture is stirred at 5° C. for 4 hrs, followed by overnight stirring at room temperature. After removal of the solvents by evaporation, the residue is redissolved in methylene chloride (100 mL) and extracted with 1N HCl (2×50 mL) and brine (2×50 mL). The organic layer is dried over magnesium sulfate and evaporated, leaving N-(4-carboxybenzyl)hexanamide as an off-white solid. The N-(4-carboxybenzyl)hexanamide product is crystallized from methanol/2N HCl, m.p. 178°-179° C.

1. customat -20° C
2. stirringAfter stirring for an additional 40 min at that temperature
3. additionAfter the addition
4. stirringthe mixture is stirred at 5° C. for 4 hrs
5. stirringstirring at room temperature
6. customAfter removal of the solvents
7. customby evaporation
8. dissolutionthe residue is redissolved in methylene chloride (100 mL)
9. extractionextracted with 1N HCl (2×50 mL) and brine (2×50 mL)
10. dry with materialThe organic layer is dried over magnesium sulfate
11. customevaporated

ORDレコード

ord-67f509762b6b41e49818d4b5225c46c2

出典データセット

uspto-grants-1988_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04771064