HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylcarbinol → S-trityl-cysteine ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylcarbinol | HCID 6457 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | S-trityl-cysteine ethyl ester | HCID 21144450 | — |
Reaction Steps
To a solution of L-cysteine ethyl ester hydrochloride (18.6 g, 0.1 mole) in 200 mL TFA was added triphenylmethanol (52 g, 0.2 mole). The resulting dark brown solution was allowed to stir for 2 h at room temperature under nitrogen. The solvent was removed in vacuo and ethanol (100 mL) added to the residue. A 1M solution of sodium ethoxide (50 mL) was added to the ethanolic solution and stirred for 90 min. during which time the solution turned cloudy. The mixture was filtered, the filtered was concentrated in vacuo to give an oily residue. Flash column chromatography using ethyl acetate:hexane (1:3) and ethyl acetate gave the desired product (containing some ethyl acetate which is difficult to remove) which was stored under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05879657 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-1a6144397df54ec986563565aa91fcf8 |
| Source note | uspto-grants-1999_03 |