HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl oxalate → Dimethyl 2-(benzyloxy)-3-oxosuccinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methyl 2-(benzyloxy)acetate | HCID 11745225 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 2-(benzyloxy)-3-oxosuccinate | HCID 59771073 | — |
Reaction Steps
A solution of methyl(benzyloxy)acetate (1 eq) and dimethyl oxalate (1.2 eq) in dry THF was cooled to −78° C. and LDA (2M in THF-heptane, 1.2 eq) was added dropwise. After stirring for an hour the cold bath was removed, and stirring was continued for an additional hour. The reaction was quenched at 0° C. by pouring into cold 1N aq HCl, and the aqueous phase was extracted with EtOAc; the organic layer was washed with brine, dried and concentrated to give a crude that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414045B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-4ccc070e1dbd42008769e0b798c38516 |
| Source note | uspto-grants-2008_08 |