HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465583Generated: October 30, 2026
HCID 10335383, compound → HCID 14986678, compound
https://huagongshe.com/reaction/465583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10335383 | HCID 10335383 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Sodium bromoacetate | HCID 23675628 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14986678 | HCID 14986678 | — |
Reaction Steps
To a solution of 4.17 g (13.8 mmol) of 5-hydroxy-8-(3-pyridyl)-1-(2-tetrahydropyranyloxy)-octane (example 37) in 30 ml dry dimethylformamide is added 17 ml (27.6 mmol) of a 1.61M solution of potassium t-butoxide in tetrahydrofuran and the resulting red solution is stirred for 0.5 h. Then the mixture is cooled to 10° and 4.9 g (30.4 mmol) of sodium bromoacetate is added followed by 40 ml dry dimethylformamide, and the reaction mixture is stirred at room temperature for 18 h. 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05153214 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-2d252ca7ac884cceaa34fe6eceaf288c |
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| Source note | uspto-grants-1992_10 |
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