HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → (S)-ethyl 3-hydroxy-4-trityloxybutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-ethyl 3,4-dihydroxybutanoate | HCID 10855622 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-ethyl 3-hydroxy-4-trityloxybutanoate | HCID 10883658 | 31% |
Reaction Steps
To (S)-ethyl 3,4-dihydroxybutanoate (1.40 g, 9.45 mmol) in methylene chloride (20 ml) were added triethylamine (1.15 g, 11.36 mmol) and DMAP (17 mg, 0.139 mmol) and the solution was cooled in ice bath. Trityl chloride (2.90 g, 10.4 mol) in methylene chloride (15 ml) was dropped to the solution under stirring and then stirred at room temperature over night. The reaction mixture was washed with saturated ammonium chloride and then saturated brine, dried on magnesium sulfate, filtered and condensed in vacuo. The residue was subjected to silica gel chromatography to give (S)-ethyl 3-hydroxy-4-trityloxybutanoate (1.11 g, yield 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06620977B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-abdd119dbf614fadb375c09ec1071e2a |
| Source note | uspto-grants-2003_09 |