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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879809Generated: October 30, 2026

Heptane → HCID 86635761, compound

https://huagongshe.com/reaction/1879809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptaneHCID 8900—
Reactant1,3-DiacetoxyacetoneHCID 243418—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
Solvent1,1-DichloroethaneHCID 6365—
SolventEthyl AcetateHCID 8857—
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 (1:1 heptane: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 numberUS08318705B2
Source datasetuspto-grants-2012_11
ORD IDord-c6e9f58a9e064437b3d7833d5cc2ecd2
Source noteuspto-grants-2012_11