HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → N-[N-trifluoroacetyl-4-(hexadecylamino)benzoyloxy]succinimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | N-trifluoroacetyl-4-(hexadecylamino)benzoic acid | HCID 20437350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-[N-trifluoroacetyl-4-(hexadecylamino)benzoyloxy]succinimide | HCID 20437360 | — |
Reaction Steps
To a stirred ice-cold solution of 18.3 g. of p-(2,2,2-trifluoro-N-hexadecylacetamido)benzoic acid in 80 ml. of dioxane is added successively 4.84 g. of N-hydroxysuccinimide and 9.16 g. of dicylohexylcarbodiimide. After 18 hours at 0°-5° C. the mixture is stirred vigorously for one hour with hexane and water and filtered. The hexane layer is washed with water, dried over magnesium sulfate, and concentrated to give an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04485105 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-123a317fa24c47769f939d8663431f36 |
| Source note | uspto-grants-1984_11 |