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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941714Generated: November 4, 2026

Hydrochloric Acid → 6-Hydroxyhexanoic Acid

https://huagongshe.com/reaction/1941714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactantepsilon-CAPROLACTONEHCID 10401—
ReactantPotassium HydroxideHCID 14797—
SolventTetrahydrofuranHCID 8028—
Product6-Hydroxyhexanoic AcidHCID 14490—

Reaction Steps

First, the synthesis of Compound 20 was preformed following the procedure reported in PCT/JP2005/004389. 6-Hydroxyhexanoic acid was synthesized by base hydrolysis of caprolactone. Caprolactone (100 g) was added to a mixture of potassium hydroxide (145 g), methanol (110 mL), and THF (390 mL). The resulting mixture was stirred at room temperature overnight. The solution was then acidified with HCl and extracted with ethyl acetate. The combined organic layers were washed with water, dried, filtered, and concentrated to obtain 6-hydroxyhexanoic acid. 1H NMR (CDCl3, 500 MHz) δ 1.44 (m, 2H), 1.60 (m, 2H), 1.68 (m, 2H), 2.37 (t, J=7.5 Hz, 2H), 3.66 (t, J=6.5 Hz, 2H), 5.80 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08388860B2
Source datasetuspto-grants-2013_03
ORD IDord-36ac30b23ff944f596ec67d93eeb3561
Source noteuspto-grants-2013_03