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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250635Generated: October 31, 2026

Sodium hydride → 1-Tert-butyl 5-ethyl 2-[(acetyloxy)acetyl]pentanedioate

https://huagongshe.com/reaction/2250635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-iodopropanoateHCID 10911297—
ReactantTert-butyl 4-(acetyloxy)-3-oxobutanoateHCID 57260374—
SolventTetrahydrofuranHCID 8028—
Product1-Tert-butyl 5-ethyl 2-[(acetyloxy)acetyl]pentanedioateHCID 5748138358.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 60% NaH (1.02 g) in THF (50 mL) was added tert-butyl 4-(acetyloxy)-3-oxobutanoate (5.00 g) under ice-water cooling and the mixture was stirred at 0° C. for 0.5 hour. To this added ethyl 3-iodopropanoate (5.54 g) and the mixture was stirred at 50° C. for 8 hours. The mixture was partitioned between AcOEt and water. The organic layer was separated, washed with brine, dried over MgSO4, and evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixture of hexane and AcOEt (20:1-3:1) to give 1-tert-butyl 5-ethyl 2-[(acetyloxy)acetyl]pentanedioate as yellow oil (4.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-d6b9ba51eb2544649fd3b323771b8747
Source noteuspto-grants-2008_01