HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503273Generated: November 1, 2026
Dibenzyl carbonate → HCID 70925639, compound
https://huagongshe.com/reaction/1503273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibenzyl carbonate | HCID 77002 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 5,5-Dimethylpyrrolidin-2-one | HCID 11126210 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70925639 | HCID 70925639 | 41% |
Reaction Steps
In a flame-dried 50 ml three necked flask under argon atmosphere were dissolved 1.27 g (10.0 mmol) of 5,5-dimethylpyrrolidin-2-one in 10 ml of dry THF. After cooling to −75° C., a 2 M solution of lithium diisopropylamide in THF (10.5 ml, 10.5 mmol) was added dropwise maintaining the temperature below −73° C. The solution was stirred for 1 h at −75° C. Then a solution of dibenzyl carbonate (2.72 g, 11.0 mmol) in 5 ml of THF was added dropwise at −75° C., allowed to warm up to r.t. and stirred for 1 h. The reaction was quenched by addition of 5 ml of saturated ammonium chloride solution. After extraction with ethyl acetate/water, drying over sodium sulfate and concentration; the residue was loaded onto a 50 g prepacked flash chromatography column. After elution with a 10% to 70% ethyl acetate in heptane gradient, the fractions containing the desired product were collected to yield 1.07 g (41%) of the title compound as a light yellow oil, MS: m/e=262.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212171B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-7edebe3fb0fb4bb6b86d225b74d1e2ab |
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| Source note | uspto-grants-2015_12 |
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