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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374446Generated: October 30, 2026

Acetic Acid → HCID 86592536, compound

https://huagongshe.com/reaction/1374446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcrylateHCID 8821—
ReactantSodium hydrideHCID 24758—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 11435600HCID 11435600—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 86592536HCID 8659253643.7%

Reaction Steps

To a solution of methyl (3S)-3-{[(allyloxy)carbonyl]amino}butanoate (2.06 g, 10.2 mmol) and ethyl acrylate (1.11 ml, 10.2 mmol) in toluene (25 ml) was added at 40° C. sodium hydride (60% suspension in oil, 0.41 g, 10.2 mmol). The mixture was stirred for 2 hours and then was poured into diluted hydrochloric acid. The solution was extracted twice with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over magnesium sulfate. The organic solvent was removed in vacuo. To the residue were added methanol (40 ml), acetic acid (0.70 ml, 12.2 mmol) and sodium cyanoborohydride (0.77 g, 12.2 mmol) and the mixture was stirred at room temperature for 20 minutes. The solvent was removed in vacuo and the residue was purified with silica gel chromatography to give a mixture (1.21 g) of 1-allyl 3-ethyl (6S)-4-hydroxy-6-methyl-1,3-piperidinedicarboxylate and 1-allyl 3-methyl (6S)-4-hydroxy-6-methyl-1,3-piperidinedicarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163936B2
Source datasetuspto-grants-2007_01
ORD IDord-44d5155f16e240ebaeedc5907d8e3f8e
Source noteuspto-grants-2007_01