Benzyl Bromide → Boc-L-Homoser-Obzl

A solution of di-tert-butylcarbonate (36.40 g, 166.8 mmol) in dioxane (100 ml) was added to a solution of (±)-α-amino-γ-butyrolactone hydrobromide (25.28 g, 138.9 mmol) in a mixture of dioxane/water=1/1 (200 ml). 20 minutes were spent in adding dropwise a solution of sodium hydroxide (12,58 g, 321.1 mmol) in water (100 ml) to the mixture with ice-cooling and with stirring. This mixture was stirred for 30 minutes with ice-cooling and then at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure. Water (300 ml) was added to the residue and the mixture was acidified by citric acid (25 g) and extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in ethanol (200 ml), and a solution of sodium hydroxide (5.44 g, 138.9 mmol) in water (33 ml) was added to the solution with ice-cooling. After this mixture was allowed to stand at room temperature overnight, it was concentrated under reduced pressure. The resulting residue was dissolved in N,N-dimethylformamide (150 ml), benzyl bromide (16.5 ml, 138.7 mmol) was added to the solution, the mixture was stirred at room temperature overnight, and then it was concentrated under reduced pressure. To the residue, a saturated aqueous solution of ammonium chloride was added and this was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the title compound (39.75 g, yield 93%) as a pale yellow oil.

1. custom20 minutes
2. temperaturecooling
3. stirringThis mixture was stirred for 30 minutes with ice-
4. temperaturecooling
5. concentrationThe reaction mixture was concentrated under reduced pressure
6. additionWater (300 ml) was added to the residue
7. extractionextracted with ethyl acetate
8. washThe organic layer was washed with water
9. dry with materialdried over anhydrous magnesium sulfate
10. concentrationconcentrated under reduced pressure
11. dissolutionThe residue was dissolved in ethanol (200 ml)
12. temperaturecooling
13. waitto stand at room temperature overnight
14. concentrationit was concentrated under reduced pressure
15. dissolutionThe resulting residue was dissolved in N,N-dimethylformamide (150 ml)
16. stirringthe mixture was stirred at room temperature overnight
17. concentrationit was concentrated under reduced pressure
18. additionTo the residue, a saturated aqueous solution of ammonium chloride was added
19. extractionthis was extracted with ethyl acetate
20. washThe organic layer was washed with water
21. dry with materialdried over anhydrous magnesium sulfate
22. concentrationconcentrated under reduced pressure

ORD record

ord-06c7152d7bf4452b8c3a3bde9a618cfa

Source dataset

uspto-grants-2004_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06673804B1