Thionyl Chloride → HCID 11086720, compound
Reaction equation
S(Cl)(Cl)=O.[CH:5](N(C(C)C)CC)(C)C.[CH3:14][O:15][C:16](=[O:31])[C@H:17]([CH2:29][OH:30])[NH:18][C:19]([O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:20]>C(O)C>[CH2:14]([O:15][C:16](=[O:31])[C@H:17]([CH2:29][OH:30])[NH:18][C:19]([O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:20])[CH3:5]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Thionyl chloride (5.25 mL, 72 mmol, 3.6 equiv.) is added dropwise to a 0° C. solution of absolute ethyl alcohol (20 ml). Diisopropyl ethylamine (3.45 ml, 19. mmol, 1 equiv.) was added and then 4.8 g of N-CBZ-L-serine methyl ester was added as a solid. Stirring is continued for 16 hours at room temperature. The ethanol and thionyl chloride are then removed by rotary evaporation and the residue is dissolved in ethyl acetate (200 mil). The organic phase is washed with 1N hydrochloric acid (50 ml) and saturated sodium bicarbonate (50 ml) and brine (20 ml). The organic layer is dried with magnesium sulfate. Rotary evaporation of the product gives an oil which is chromatographed on silica gel with hexane/ethyl acetate (3:1) to give N-CBZ-L-serine ethyl ester.
Workup
- customThe ethanol and thionyl chloride are then removed by rotary evaporation
- dissolutionthe residue is dissolved in ethyl acetate (200 mil)
- washThe organic phase is washed with 1N hydrochloric acid (50 ml) and saturated sodium bicarbonate (50 ml) and brine (20 ml)
- dry with materialThe organic layer is dried with magnesium sulfate
- customRotary evaporation of the product
- customgives an oil which
- customis chromatographed on silica gel with hexane/ethyl acetate (3:1)
Sources & evidence
- ORD record
- ord-4f9f07c918db455d9c366a34677a1a3a
- Source dataset
- uspto-grants-1986_11
- Patent number
- US04622417
Reaction notes
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