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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBenzyl tert-butyl malonateHCID 2736712—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductDibenzyl 3(RS)-tert-butoxycarbonyl-2(R)-isobutylsuccinateHCID 1866080489%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284914B1
Source datasetuspto-grants-2001_09
ORD IDord-f0fddce99f0549f1a91fd0b01bf7c019
Source noteuspto-grants-2001_09