HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2S,3S)-2-benzyloxy-5-(1-naphthyl)-3-pentyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (2S,3S)-2-benzyloxy-5-(1-naphthyl)pentan-3-ol | HCID 57094200 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S,3S)-2-benzyloxy-5-(1-naphthyl)-3-pentyl methanesulfonate | HCID 56983838 | 107.4% |
Reaction Conditions
| Temperature | 4 °C |
|---|
Reaction Steps
To an ice-cooled solution of (2S,3S)-2-benzyloxy-5-(1-naphthyl)pentan-3-ol (obtained in Preparation 26) (7.43 g) in dichloromethane (100 ml) was added methanesulfonyl chloride (2.15 ml) followed by triethylamine (3.88 ml). The mixture was stirred at 4° C. for 40 min. After being diluted with dichloromethane, the mixture was washed with water and brine, dried and concentrated in vacuo to give (2S,3S)-2-benzyloxy-5-(1-naphthyl)-3-pentyl methanesulfonate (9.92 g, 107.4%) as an oil. The product was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06359145B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-a20ce673e54e486cb67530a62c074fd5 |
| Source note | uspto-grants-2002_03 |