HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595072Generated: October 30, 2026
Ethyl Acetate → Dibenzyl 3(RS)-tert-butoxycarbonyl-2(R)-isobutylsuccinate
https://huagongshe.com/reaction/1595072
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzyl tert-butyl malonate | HCID 2736712 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dibenzyl 3(RS)-tert-butoxycarbonyl-2(R)-isobutylsuccinate | HCID 18660804 | 89% |
Reaction Steps
Benzyl tert-butyl malonate (24.9 g, 99.6 mmol) was dissolved in DMF (60 ml) and added portion wise with potassium tert-butoxide (13.4 g, 120 mmol) at 0° C. under stirring. The mixture was stirred at room temperature for 1 hour, then cooled to 0° C., and dropped in 1 hour with the solution of the Example 3-a compound (28.4 g, 99.6 mmol) dissolved in DMF (60 ml). After the reaction mixture was stirred at 5° C. overnight, it was added with AcOEt (2 l) and washed with a saturated aqueous solution of NaCl, 1N-HCl, a saturated aqueous solution of NaHCO3 and then the saturated aqueous solution of NaCl two times respectively. The organic layer was dried over anhydrous MgSO4, evaporated under reduced pressure and purified by column chromatography (silica gel; 750 g, elution with the mixed solvent; n-hexane:AcOEt=20:1), giving the title compound (40.0 g, 89%) of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06284914B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-f0fddce99f0549f1a91fd0b01bf7c019 |
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| Source note | uspto-grants-2001_09 |
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