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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489840Generated: October 29, 2026

Hydrochloric Acid → 6-Hydroxyhexanoic Acid

https://huagongshe.com/reaction/1489840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6-Methyloxan-2-oneHCID 13204—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Hydroxyhexanoic AcidHCID 1449082.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 12.0 g of ε-hexanolactone in 20 ml of ethanol was added a solution of 11.7 g of potassium hydroxide in 20 ml of water under ice-cooling and the reaction mixture was stirred for 2.5 hours at 40° C. After reaction, the reaction mixture was adjusted to pH 9 by adding 1N-HCl solution and washed with ethyl acetate (twice). The aqueous layer was concentrated under reduced pressure and the residue was adjusted to pH 1 by adding 1N-HCl solution and extracted by ethyl acetate. The organic layer was dried over magnesium sulfate and the solvent was removed under reduced pressure to give 11.5 g of 6-hydroxyhexanoic acid. A mixture of 1 g of 6-hydroxyhexanoic acid obtained above, 0.72 mg of sodium bicarbonate in 20 ml of water was stirred for 15 minutes. After reaction, the solvent was removed and the resulting residue was washed with acetonitrile to give 1.24 g of sodibm 6-hydroxyhexanoic acid. Then, 276 mg of this compound was dissolved in 2.7 ml of dimethylformamide and to this solution was added 161 mg of methoxymethyl chloride and the reaction mixture was stirred for 1.5 hours at room temperature. After adding 10 ml of ethyl acetate to the reaction mixture, the organic layer was washed with saline, saturated sodium bicarbonate aqueous solution and saline respectively and dried over magnesium sulfate. The solvent was removed to give 190 mg (59%) of methoxymethyl 6-hydroxyhexanoate [Compound (15)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679790
Source datasetuspto-grants-1997_10
ORD IDord-08b25579281f4310960c0b8d105244a6
Source noteuspto-grants-1997_10