HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → Ethyl 2-((benzyl(cyclopentyl)amino)methyl)-2-fluorobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Ethyl 2-((benzyl(cyclopentyl)amino)methyl)-2-hydroxybutanoate | HCID 57955651 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-((benzyl(cyclopentyl)amino)methyl)-2-fluorobutanoate | HCID 57955532 | 75.2% |
Reaction Steps
To ethyl 2-((benzyl(cyclopentyl)amino)methyl)-2-hydroxybutanoate (2.9 g, 9.1 mmol) in 30 ml of dichlormethane at −78° C., was added DAST (2.4 ml, 18 mmol) dropwise. The reaction mixture was gradually warmed up to room temperature and stirred for 1 h. It was then diluted to dichloromethane, washed by NaHCO3, brine and water. Organic extract dried and concentrated to a residue, which was purified on silica gel column chromatographically (Hex/EtOAc=40:1 to 20:1) to give 2.2 g product (75%) as light yellow liquid. [M+H] calc'd for C19H28FNO2, 322; found 322.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318727B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-acd205d4b9cc4f199a3830350acbb541 |
| Source note | uspto-grants-2012_11 |