HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Methyl (2S)-2-hydroxy-3-methoxy-3,3-diphenylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (2S)-2-Hydroxy-3-methoxy-3,3-diphenylpropanoic acid | HCID 15380898 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl (2S)-2-hydroxy-3-methoxy-3,3-diphenylpropanoate | HCID 10636938 | — |
Reaction Steps
54.4 g (200 mmol) of (S)-2-hydroxy-3-methoxy-3,3-diphenylpropionic acid were introduced with 10.8 g (200 mmol) of sodium methoxide into 300 ml of DMF. 21 ml (210 mmol) of dimethylsulfate were added dropwise to this suspension over 15 minutes, during which the temperature rises to 50° C. and the suspension becomes mobile. The mixture was stirred overnight and then added to 1.5 l of water and ice. The aqueous phase was extracted twice with 500 ml of ether, and the ether phase was in turn washed with 200 ml of water twice. The organic phase was dried over magnesium sulfate, the desiccant was filtered off, and the solvent was distilled off. 55.8 g of an oil were isolated and were immediately processed further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06670367B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-92f79e17777b490fa5f4ccb530e86fb3 |
| Source note | uspto-grants-2003_12 |