HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856397Generated: October 27, 2026
Potassium Hydroxide → 2-Hydroxymethyl-3-(5-carboethoxypentyloxy)-6-(trimethylacetoxymethyl)-4-pyrone
https://huagongshe.com/reaction/1856397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 6-iodohexanoate | HCID 10880140 | — |
| Reactant | 2-Hydroxymethyl-3-hydroxy-6-(trimethylacetoxymethyl)-4-pyrone | HCID 23344868 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxymethyl-3-(5-carboethoxypentyloxy)-6-(trimethylacetoxymethyl)-4-pyrone | HCID 23344856 | 27% |
Reaction Steps
To a solution of 1.84 g (0.028 mole) of potassium hydroxide in 38 ml of ethanol and 10 ml of water was added 6.76 g (0.026 mole) of 2-hydroxymethyl-3-hydroxy-6-(trimethylacetoxymethyl)-4-pyrone, and the resulting mixture heated to 50°. An 8.3 g (0.03 mole) portion of ethyl 6-iodohexanoate was then added and the resulting clear solution heated at reflux for 7 hr under a nitrogen atmosphere. 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 2.9 g (27%) of oily product, 2-hydroxy-3-(5-carboethoxypentyloxy)-6-trimethylacetoxymethyl)-4-pyrone. NMR (CDCl3): δ1.22 (3H, t, J=7 Hz), 1.23 (9H, s), 2.30 (2H, t, J=5.5 Hz), 6.32 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04219483 |
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| Source dataset | uspto-grants-1980_08 |
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| ORD ID | ord-2328eea4223e46ac92ad20957dcb9bb3 |
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| Source note | uspto-grants-1980_08 |
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