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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703534Generated: October 25, 2026

Tetrahydropyranyl ether → Tetrahydropyranyl ether

https://huagongshe.com/reaction/1703534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydropyranyl etherHCID 263182—
Reactant6-Ketoprostaglandin F1 alphaHCID 5280888—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
ProductTetrahydropyranyl etherHCID 263182—
Product6-Keto-PGE1HCID 5280889—

Reaction Steps

The reaction product from part A, containing 6-keto-PGF1α, bis(tetrahydropyranyl)ether, methyl ester corresponding to formula IV, is oxidized to compound V. A composite from several lots, weighing 0.93 g., in 20 ml. of acetone is treated at -10° C. with 2.0 ml. of Jones reagent. After stirring for 1.5 hr. the reaction mixture is quenched with isopropanol and extracted with diethyl ether. The extract is washed with brine, dried, and concentrated. The residue is subjected to silica gel chromatography, eluting with ethyl acetate (20-50%)-Skellysolve B to yield the formula-V 6-keto-PGE1, bis(tetrahydropyranyl)ether, methyl ester, 0.52 g., having Rf 0.52 (TLC on silica gel in ethyl acetate-Skellysolve B (1:1)); and infrared peaks at 1745 and 1725 cm-1 (free of OH at 3000-3500).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124601
Source datasetuspto-grants-1978_11
ORD IDord-ddb5f52ad53f43148906cd287b3f63a4
Source noteuspto-grants-1978_11