HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bicarbonate → Di-tert-butyl (2s,5s)-5-hydroxyethylpyrrolidine-1,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | di-tert-butyl (2S,5S)-5-ethoxycarbonylmethylpyrrolidine-1,2-dicarboxylate | HCID 91432523 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Di-tert-butyl (2s,5s)-5-hydroxyethylpyrrolidine-1,2-dicarboxylate | HCID 91484630 | — |
Reaction Steps
43 g of the product from 1d were dissolved in 300 ml of diethyl ether. A solution of 3.1 g of lithium borohydride in 300 ml of diethyl ether was added dropwise thereto. The mixture was stirred for 6 h and the reaction was stopped by cautious addition of 300 ml of a saturated potassium bicarbonate solution. The phases were separated and the organic phase was washed with 250 ml of a saturated sodium chloride solution. The organic phase was dried with sodium sulfate, and the solvent was removed in vacuo. The residue was chromatographed on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094800B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-2ee3358ec00f4d3a99109190e3ee13ea |
| Source note | uspto-grants-2006_08 |