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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494125Generated: November 4, 2026

HCID 10335383, compound → HCID 14986678, compound

https://huagongshe.com/reaction/1494125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10335383HCID 10335383—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantSodium bromoacetateHCID 23675628—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14986678HCID 14986678—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 4.17 g (13.8 mmol) of 5-hydroxy-8-(3-pyridyl)-1-(2-tetrahydropyranyloxy)-octane in 30 mL dry dimethylformamide is added 17 mL (27.6 mmol) of a 1.61 M solution of potassium t-butoxide in tetrahydrofuran and the resulting red solution is stirred for 0.5 hour. Then the mixture is cooled to 10° C. and 4.9 g (30.4 mmol) of sodium bromoacetate is added followed by 40 mL dry dimethylformamide, and the reaction mixture stirred at room temperature for 18 hours. The reaction mixture is diluted with ether and water. The ether layer is separated and the aqueous phase is adjusted to pH=6.5 using 1N aqueous hydrochloric acid. The resulting solution is extracted thrice with ethyl acetate. The aqueous phase is again adjusted to pH=6.5 and extracted again. The combined organic phase is washed with brine, dried, filtered, and concentrated to give 8-hydroxy-4-[3-(3-pyridyl)propyl]-3-oxa-octanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-4d1cc2daee794f5eb2d11a83db94b30c
Source noteuspto-grants-1991_06