Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178418600 | HCID 178418600 | — |
| Product | HCID 178443800 | HCID 178443800 | 85% |
Reaction Steps
One millimole thionyl chloride was added to a stirred suspension of one millimole L-arginine free base in 50 mL of octanol under nitrogen. The mixture was heated to 90° C, and the temperature was maintained with stirring for 2 hours. The mixture was cooled to 60° C, one more equivalent of thionyl chloride was added, and the mixture was stirred at 60° C. for an additional 2 hours, at which time the reaction was seen to be complete by TLC (performed as described in Example 33). Excess thionyl chloride was allowed to evaporate. Then, the solution was cooled to room temperature, and 250 ml diethyl ether was added. Washing of the resultant soft white precipitate with saturated sodium bicarbonate solution gave a white solid. Filtration of this suspension and washing of the filtrate with saturated sodium bicarbonate solution (3× with 20 ml), water (3× with 20 ml), acetone (3× with 20 ml) and diethyl ether (3× with 20 ml) gave arginine octyl ester. The yield was 85%. FAB mass spectrometry gave the expected parameters for arginine octyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613358B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-b8c4e133d68640978436e90839361dd8 |
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| Source note | uspto-grants-2003_09 |
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