HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Dimethyl (1R,2S)-3-oxocyclopentane-1,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethyl butane-1,2,4-tricarboxylate | HCID 543737 | — |
| Reactant | HCID 12576408 | HCID 12576408 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | Dimethyl (1R,2S)-3-oxocyclopentane-1,2-dicarboxylate | HCID 70256462 | — |
Reaction Steps
The method of cyclizing 1,2,4-tricarbomethoxy butane, in solution in dry p-xylene containing a trace of methanol, with excess of a suspension in dry p-xylene of a dispersion of an alkali metal hydride in mineral oil, the tricarbomethoxybutane being added portionwise to the alkali metal hydride suspension with mixing at a reaction temperature of about 20° to about 40° C. for a time sufficient to form trans-2,3-dicarbomethoxycyclopentanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125556 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-badb2d26f6ef4945ada43423442580e4 |
| Source note | uspto-grants-1978_11 |