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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630451Generated: October 31, 2026

Ethyl Acetate → HCID 86635761, compound

https://huagongshe.com/reaction/1630451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,3-DiacetoxyacetoneHCID 243418—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 86635761HCID 8663576117%

Reaction Steps

To a solution of 3-(acetyloxy)-2-oxopropyl acetate (4.54 g, 26 mmol) in dichloroethane (75 ml) was added tert-butyl 2-(methylamino)acetate HCl. After stirring for 10 minutes sodium triacetoxyborohydride (8.3 g, 39 mmol) was added and stirring was continued for 18 hours and monitored by TLC (1:1heptane:EtOAc). The reaction was quenched by the addition of saturated sodium hydrogen carbonate solution and the crude product was extracted into dichloromethane. The organic phase was separated, dried over MgSO4, filtered and concentrated in vacuo. The title compound was purified by silica column chromatography eluting with 0-20% EtOAc:Hept to yield the title compound (1.32 g, 17% yield). 1H NMR (250 MHz, CHLOROFORM-d) δ 4.07-4.33 (4H, m), 3.34 (2H, s), 3.23 (1H, t, 5.9 Hz), 2.49 (3H, s), 1.99-2.19 (6H, m), 1.33-1.55 (9H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791134B2
Source datasetuspto-grants-2014_07
ORD IDord-3ad16382816a42a5876e9868cfdc016f
Source noteuspto-grants-2014_07