Carbon Disulfide → p-Nitrobenzyl 2-(4-hydroxy-1,3-dithiolan-2-ylidene)-2-(4-methylthio-2-azetidinon-1-yl)acetate

Temperature

-78 °C

A solution of butyllithium in hexane (2.4 ml, 1.63 mmoles/ml) was added to a solution of hexamethyldisilazene (740 μl) in tetrahydrofuran (12 ml) at room temperature, and then the mixture was stirred for 30 minutes. The solution was cooled to -78° C. and a solution of p-nitrobenzyl (4-methylthio-2-azetidinon-1-yl)acetate (620 mg) in tetrahydrofuran (5 ml) was added thereto, and the mixture was stirred for 10 minutes. Carbon disulphide (181 μl) was added to the resulting mixture, which was then stirred for 1 hour. A solution of iodoacetaldehyde (503 mg) in tetrahydrofuran was added to the solution, after which the mixture was stirred at -78° C. for 2 hours. The reaction mixture was then diluted with acetic acid (606 μl) and ethyl acetate and washed successively with an aqueous solution of sodium chloride, an aqueous solution of sodium bicarbonate and again an aqueous solution of sodium chloride and dried over anhydrous sodium sulphate. The solvent was distilled off under reduced pressure and the resulting residue was dissolved in tetrahydrofuran (4 ml). A drop of p-toluenesulphonic acid was added to the solution, which was then stirred at room temperature for 1.5 hours. The solvent was distilled off under reduced pressure and the resulting residue was purified by column chromatography (eluent: a 1:1 by volume mixture of benzene and ethyl acetate), to give 733 mg of the desired product as a foamy substance.

1. stirringthe mixture was stirred for 10 minutes
2. stirringwas then stirred for 1 hour
3. stirringafter which the mixture was stirred at -78° C. for 2 hours
4. washwashed successively with an aqueous solution of sodium chloride
5. dry with materialan aqueous solution of sodium bicarbonate and again an aqueous solution of sodium chloride and dried over anhydrous sodium sulphate
6. distillationThe solvent was distilled off under reduced pressure
7. dissolutionthe resulting residue was dissolved in tetrahydrofuran (4 ml)
8. additionA drop of p-toluenesulphonic acid was added to the solution, which
9. stirringwas then stirred at room temperature for 1.5 hours
10. distillationThe solvent was distilled off under reduced pressure
11. customthe resulting residue was purified by column chromatography (eluent
12. additiona 1:1 by volume mixture of benzene and ethyl acetate),

ORD record

ord-c8652b43724643f19a800a57d17fe79c

Source dataset

uspto-grants-1987_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04639441