Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | N-tert-Butoxycarbonyl-L-threonine | HCID 2724766 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 14308410 | HCID 14308410 | 85% |
Reaction Steps
To a stirred suspension of Boc-Thr-OH (21.91 g, 0.1 mol) in EtOAc (200 ml) at 0° C., TEA (14 ml, 0.1 mol) and bromoacetophenone (19.0 g, 0.1 mol) were added. The reaction mixture was allowed to warm to 20° C., stirred for 2 days and then diluted with EtOAc (500 ml). After washing successively with aq HCl (200 ml, 0.1 N), H2O (100 ml), aq NaBCO3 (200 ml, 1 N) and brine (200 ml), drying (Na2SO4), filtered and concentrated in vacuo, the residue was triturated with Et2O and filtered. The resulting solid was dried in the dark to yield D3 (28.6 g, 85%). Rf=0.55 (hex-EtOAc 1:1, silica); M.p.=114.2° C.; [α]D22 −29.4 (c 2, EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07348310B2 |
|---|
| Source dataset | uspto-grants-2008_03 |
|---|
| ORD ID | ord-4978044b56df48d38ad747e709bf0ff0 |
|---|
| Source note | uspto-grants-2008_03 |
|---|