HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (1S,2R)-3-(benzyloxy)-1-(2-chlorophenyl)-1-hydroxypropan-2-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonium cerium-nitrate | HCID 57418452 | — |
| Reactant | (2R,3R)-2-(benzyloxymethyl)-3-(2-chlorophenyl)oxirane | HCID 118140949 | — |
| Product | (1S,2R)-3-(benzyloxy)-1-(2-chlorophenyl)-1-hydroxypropan-2-yl acetate | HCID 118379240 | 34% |
Reaction Steps
To a solution of (±)-2-(benzyloxymethyl)-3-(2-chlorophenyl)oxirane (Preparation example 373, 2.9 g, 10.55 mmole) in Acetic acid (55 mL) was added Cerium Ammonium Nitrate (1.15 g, 2.11 mmole) at room temperature. The mixture was stirred for 18 hr at room temperature. The TLC showed complete consumption of SM. The reaction mixture was quenched with sat'NaHCO3 to pH7 at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica ge column to produce the title compound (1.2 g, 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221783B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-659fa5bdb0e34050a93ddaef772eba19 |
| Source note | uspto-grants-2015_12 |