HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → N-(Triphenylmethyl)-L-serine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Serine, methyl ester, hydrochloride (1:1) | HCID 2723730 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(Triphenylmethyl)-L-serine methyl ester | HCID 7128367 | 58% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 10.75 g (38.56 mmol) of trityl chloride is added, at 0° C., to a solution of 6 g (38.56 mmol) of L-serine methyl ester hydrochloride and 7.8 g (77.12 mmol) of triethylamine in absolute THF and this solution is left to stir at 0° C. for 4 h and then at room temperature for 2 days. The solvent is removed in vacuo and the residue is partitioned between dichloromethane and a 10% aqueous solution of citric acid. The phases are separated and the organic phase is washed with water and dried over sodium sulfate. Following filtration, the solvent is removed in vacuo and the residue is chromatographed through silica gel using heptane/ethyl acetate=6/4. 8 g (58%) of (34.3) are obtained after concentrating the product fractions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218415B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-5f308fcb1fbd4fb9bebcb139bbfe14d8 |
| Source note | uspto-grants-2001_04 |