HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tritylamine → Fmoc-Asn(Trt)-OH
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tritylamine | HCID 138598 | — |
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | Fmoc-Asp-OBzl | HCID 11224591 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Fmoc-Asn(Trt)-OH | HCID 640248 | — |
Reaction Steps
0.8 ml of 1-chloro-N,N,2-trimethyl-prop-1-enylamine (A. Devos et al., J. Chem. Soc., Chem. Commun., Vol. 1979, p. 1180) is added to a stirred solution of 2.09 g of Fmoc-Asp-OBzl in 20 ml of 1,2-dichloroethane at 0° under an argon atmosphere. After 10 minutes, a solution of 1.2 g of tritylamine in 4 ml of 1,2-dichloroethane is added, and then the mixture is stirred for 2 hours, diluted with ethyl acetate and washed with water. The organic phase is dried and evaporated. The residue is taken up in chloroform and chromatographed on 250 g of silica gel. The fractions containing the Fmoc-Asn(Trt)-OBzl are combined and evaporated; the product is obtained as an amorphous foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05324833 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-77092f084bd54ee4913616dde60a2a08 |
| Source note | uspto-grants-1994_06 |