HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163261Generated: October 25, 2026
Potassium Hydroxide → 2-Hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyrone
https://huagongshe.com/reaction/2163261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one | HCID 9869622 | — |
| Reactant | Ethyl 6-iodohexanoate | HCID 10880140 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyrone | HCID 23344855 | 54% |
Reaction Steps
To a solution of 2.75 g (0.042 mole) of potassium hydroxide in 38 ml of ethanol and 10 ml of water was added 5.93 g (0.042 mole) of 2-hydroxymethyl-3-hydroxy-4-pyrone, and the resulting mixture heated to 50°. A 12.4 g (0.046 mole) portion of ethyl 6-iodohexanoate was then added and the resulting clear solution heated at reflux for 7 hr under a nitrogen atomsphere. Removal of the ethanol under reduced pressure left a residue which was dissolved in methylene chloride. The organic solution was washed successively with aqueous NaHCO3 and saturated brine, was dried over magnesium sulfate, and was evaporated to afford a viscous oil. This material was chromatographed on silica gel eluting with ethyl acetate to give 6.34 g (54%) of oily product, 2-hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyrone: NMR (CDCl3): δ1.22 (3H, t, J = 7Hz), 2.30 (2H, t, J = 5.5 Hz), 4.63 (2H, s), 6.35 (1H, d, J = 6 Hz), 7.73 (1H, d, J = 6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04132847 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-c5639ed8186d4c33b3e3c914a0c3f87e |
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| Source note | uspto-grants-1979_01 |
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