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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789247Generated: October 30, 2026

Propionic Acid → ethyl[(1RS,3S)-2,2-dimethyl-6-methylene-3-tetrahydropyranyloxycyclohexyl]acetate

https://huagongshe.com/reaction/1789247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic AcidHCID 1032—
Reactant(4S)-3,3-dimethyl-4-tetrahydropyranyloxy-1-hydroxymethylcyclohexeneHCID 13924113—
ReactantEthyl ortho-acetateHCID 86598186—
Productethyl[(1RS,3S)-2,2-dimethyl-6-methylene-3-tetrahydropyranyloxycyclohexyl]acetateHCID 1392411596%

Reaction Conditions

Temperature140 °C

Reaction Steps

Compound (9) (9.45 g, 39.3 mmoles) and propionic acid were dissolved in newly distilled ethyl ortho-acetate (51.0 g, 314 mmoles). The solution was stirred at 140° C. for 6 hours while distilling off ethanol. Ethyl ortho-acetate was removed from the resulting reaction mixture, and the residue was concentrated. After cooling, the residue was diluted with ether. The ether solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and then with an aqueous solution of sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (200 g of silica gel; n-hexane/ethyl acetate) to give a compound (10) as a mixture of the (1S,3S)-isomer and (1R,3S)-isomer (11.7 g, 37.7 mmoles, yield 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04687863
Source datasetuspto-grants-1987_08
ORD IDord-43d5bbdfb3f54ea3b1458d64c905aca6
Source noteuspto-grants-1987_08