Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | HCID 178427284 | HCID 178427284 | — |
| Reactant | HCID 178482655 | HCID 178482655 | — |
| Solvent | 1-Hexanol | HCID 8103 | — |
| Product | HCID 178445076 | HCID 178445076 | 95% |
Reaction Steps
A mixture of 1.0 gram of N2 -dansyl-L-arginine and 1.4 gram of p-toluenesulfonic acid monohydride in 10 ml of n-hexyl alcohol was heated for 30 minutes at 100° C. To the thus obtained clear solution, 100 ml of benzene was added, and the mixture was refluxed for 3 hours, removing water by azeotropic distillation. After the solvent was removed by distillation, 50 ml of ethyl ether and 50 ml of petroleum ether were added to the residue to give a crystalline mass. Crystallization from acetone gave N2 -dansyl-L-arginine n-hexyl ester di(p-toluenesulfonate) in 95% yield; mp. 190°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04227006 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-ab33d492c18b4706940d12e9106a6072 |
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| Source note | uspto-grants-1980_10 |
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